Example of documentation template for Lab Management Process in IATF

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Lab Management in IATF. As each business is different, additional documents or revisions would be required to meet your organization’s specific needs, requirements, context, risk profile, etc. ​​If after reading through all of these documents, you feel like you still need a consulting partner to help you develop your new documents – Contact Us. We’re always looking for interesting new clients and projects.

1.0 Process Approach for Lab Management Process

2.0 Turtle Diagram for Lab Management Process

 3.0 Laboratory Scope

As On Date:                                                     Laboratory : Physical / Chemical / Standard Room

S No.Category of Tests / Calibration Done In Lab. / Std RoomInstrument UsedReference / Limit SamplesMethod of TestEnvironment ConditionCompetency of PersonnelCapability of Instrument
 Temp.HumidityQualificationExperience.In House LabExternal Lab
           
           
           
           
           
           
           
           
           

                                                                                                Approved By:

4.0 Laboratory Personal Qualification Data

SR.NO  NAMEDATE OF JOININGEDUCATIONAL QUALIFICATIONLAB-EXPEREANCE BEFOR JOININGTRAINING RECEIVEDNAME OF TESTS FOR WHICH QUALIFIEDAPPROVED BY & DATE
                                            

5.0 List of Qualified External Lab.

S.No Name of the LaboratoryAccredited ByQualified CriteriaAddressContact PersonPhone No.
       
       
       
       
       
       
       
       
       
       

Example of documentation template for Calibration of Equipment Process in IATF

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Calibration of Equipment in IATF. As each business is different, additional documents or revisions would be required to meet your organization’s specific needs, requirements, context, risk profile, etc. ​​If after reading through all of these documents, you feel like you still need a consulting partner to help you develop your new documents – Contact Us. We’re always looking for interesting new clients and projects.

1.0 Process Approach for calibration of Equipment process

Turtle Diagram for calibration of Equipment process

3.0 Annual calibration Plan

YEAR :
Sr. No.Instruments NameFrequencyJanFeb.MarAprMayJuneJulyAugSepOctNovDecRemarks
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
  
  
PREPARED BY          Approved By

4.0 In-House Calibration Certificate

  CERT. NO. ——————-   DATE              ——————-
Equipment I.D.:Made/Make:
Manufacturer:Model No :
Type of Machine:Serial No.:
Drive:Physical Condition:
Referance Procedure:Revision Status:
  CALIBRATION DATA
  Regulator Scale Marking   Measured marking  Variation     Remarks
    
    
    
    
    
    
    
  MASTER EQUIPMENT TRACEBILITY
Equipment Type 
Equipment I.D. No. 
Calibration By. 
Calibration Certificate No. 
 
Calibrated By:Certified by:
Name:Name:
Signature:Signature:
DateDate:
Issue.No./Date: xx/xx.xx.xxxx
Rev.No/Rev.Date:xx/xx.xx.xxxx

Example of documentation template for Information Technology Process in IATF

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Information Technology Process in IATF. As each business is different, additional documents or revisions would be required to meet your organization’s specific needs, requirements, context, risk profile, etc. ​​If after reading through all of these documents, you feel like you still need a consulting partner to help you develop your new documents – Contact Us. We’re always looking for interesting new clients and projects.

1.0 Process Approach for Information Technology Process

2.0 Turtle diagram of for Information Technology Process

1. Master list of IT assets

  MASTER LIST
Sr. No.NameUser_NameDepartmentI.P. AddressLocationConfigurationTypePurchase date
         
         
         
         
         
         
         
         
         
         
         
         
         
         
         
         
         
Prepared By:   Approved By:

2. Breakdown slip

Department :Date :
Equipment Name :Equipment No.:
STATUS BEFORE MAINTENANCE
Problem Observed/Condition of Equipment :  Breakdown Date:
  Breakdown Time:
    Signature of concerned dept.
STATUS AFTER MAINTENANCE
Handover Date :Equipment Status            Signature of concerned dept.
Handover Time :  GOOD  YES /  NO
  Total Breakdown Time :  TEMPORARY WORKING  YES /  NO
ANALYSIS
Immediate Action :  OCCURANCE
Repeat  YES / NO
First time  YES / NO
Root Cause :
Counter measure after determining root cause of breakdown :
MAINTENANCE COSTREMARKS
Replacement Part Cost(Rs.)  
Man power Cost(Rs.) 
Subcontractor  Cost(Rs.) 
TOTAL COST (Rs.) 
      Attended By                                                                               Sign (Incharge)
      Prepared By                                                                                                Approved by

3.0 IT Equipment History Card

EQUIPMENT NAME:Equipment No Equipment Make
SR. No.Problem Detail Location Breakdown Time Spare part Consummation Action Taken REMARKS
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       

4.0

PREVENTIVE MAINTENANCE SCHEDULE
Sr.No.Equipment nameEquipment IDPlan for Year xxxx-xx
AprMayJuneJulAugSepOctNovDecJanFebMar
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
    Prepared By:         Approved By:

4.0 PREVENTIVE MAINTENANCE SCHEDULE

Sr.No.Equipment nameEquipment IDPlan for Year xxxx-xx
AprMayJuneJulAugSepOctNovDecJanFebMar
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
    Prepared By:         Approved By:

5.0 List of critical spares

  S.NO.  Name of parts  Min.stock level  Max.Stock Level  Remarks
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
  PREPARED BY   Approved By

6.0 Preventive Maintenance checklist

Computer Name:                        Date:   Monthly (By I.T. Department)
Sr.No.Work To be DoneYesNo
1Scan through antivirus and update the latest  antivirus.  
2Clean the computer, telephone and other accessories.  
3Delete all unnecessary files from your computer.  
4Check the all cables connected with the computer.  
5Check the function of the computer related to network, outlook or any another software used by user.  
6Clear all temp file to cleaner software.  
7Run scandisk .  
8Clean and check every hardware as well as software.  
9Also verify the backup with master schedule backup.  
10Make restore point of the computer.  
11Make backup manually . Also take back up on CD or DVD.  
12Clean with blower  
  Prepared By:                                                                                                     Approved By:

Example of documentation template for Process to Manage the use of alternate control methods in IATF

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Process to Manage the use of alternate control methods in IATF. As each business is different, additional documents or revisions would be required to meet your organization’s specific needs, requirements, context, risk profile, etc. ​​If after reading through all of these documents, you feel like you still need a consulting partner to help you develop your new documents – Contact Us. We’re always looking for interesting new clients and projects.

1.0 Process Approach of Process to Manage the use of alternate control methods

2.0 Turtle Diagram of Process to Manage the use of alternate control methods

3.0 List of Alternate Control Method

S.No.DEPT NAMEPROCESS NAMEEXISTING METHODALTERNATE METHODREMARKS
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
PREPARED BY   APPROVED BY

Example of documentation template for Process of Facility Planning & Deployment in IATF

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Process of Facility Planning & Deployment in IATF. As each business is different, additional documents or revisions would be required to meet your organization’s specific needs, requirements, context, risk profile, etc. ​​If after reading through all of these documents, you feel like you still need a consulting partner to help you develop your new documents – Contact Us. We’re always looking for interesting new clients and projects.

1.0 Process Approach of Process of Facility Planning & Deployment

2.0 Turtle diagram of Process of Facility Planning & Deployment

3.0 Communication Matrix

Department :    ____________                                  As on Date : ___/___/___  
S.No.Communication TitleFormat/ ModeFrequency.Department / Function
CustomerMarketingProductionPPC & DispatchEngg.Tool RoomHRMaterialsQualityMRLabPlant Maintenance
              
                
                
                
                
                
                
                
              
                
                
                
                
                
                
 
Include all types of applicable Communications emerging from the department  and communicated to other departments including Management Representative and Customer e.g. Objectives & Quality Policy,
Progress on Continual Improvement Projects, Non-conformance, Conformance Reports, Audit Results for effectiveness of Management Systems, Corrective and Preventive Actions, Supplier Performance, Customer & Statutory / Regulatory Requirements.
Mode of communication may be either through Dept meetings, Display at Notice Boards, Circulation of Hard Copy formats, LAN, Verbal  or through Company Bulletins / News Letters.
Signature
(Department Head)

4.0 PROJECT IDENTIFICATION FOR IMPROVEMENTS & APPROVAL

5.0 Action Plan for Implementing Improvement Project

Name of Project :

Expected Improvements from Project if any  :

Project Team Members (Including Team Leader)  :

Target Date for Completion of Project    :

Action Plan:

S. No.ActivityResponsibilityTargetReviewed By
   IIIIIIIVV 
              
          
              
          
              
          
              
          
              
          
              
          
              
          
              
          
              
          
              
          
              
          

Prepared By:                                                                                         Approved By:

6.0 Resource Planning

Name of Department:                                                                                

Monitoring Details
NameDateSign
   
   
   
   
S. No.Required InfrastructureRequiredAvailableAdditional RequiredAPPLICABLE PROCESSES
Communication         
A.INFRASTRUCTURE RELATED TO BUILDING, WORK SPACE, HARDWARE, SOFTWARE, TRANSPORTATION, UTILITY, COMMUNICATION MEANS, CHECKING AIDS
               
               
               
               
               
               
               
               
               
               
               
               
               
B.WORK ENVIRONMENT/ SUPPORT FACILITIES RELATED TO TEMPERATURE, HUMIDTY, HOUSE KEEPING, LIGHTING, PERSONNEL PROTECTIVE EQUIPMENT (PPE)
               
               
               
               
               
               
               

NOTE:      IN CASE, INFRA-STRUCTURE IS NOT OK TO MEET OBJECTIVES / PERFORMANCE INDICATORS OR NEW TO BE INSTALLED, MAKE ACTION PLANS WITH TARGET DATE AND RESPONSIBILITY

Example of documentation template for Process of Product Safety in IATF

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Process of Product Safety in IATF. As each business is different, additional documents or revisions would be required to meet your organization’s specific needs, requirements, context, risk profile, etc. ​​If after reading through all of these documents, you feel like you still need a consulting partner to help you develop your new documents – Contact Us. We’re always looking for interesting new clients and projects.

Example of documentation template for Process of Identification of special characteristics in IATF

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Process of Identification of special characteristics in IATF. As each business is different, additional documents or revisions would be required to meet your organization’s specific needs, requirements, context, risk profile, etc. ​​If after reading through all of these documents, you feel like you still need a consulting partner to help you develop your new documents – Contact Us. We’re always looking for interesting new clients and projects.

1.0 Process Approach for process of Identification of special characteristics

2) Turtle Diagram for process of Identification of special characteristics

3) LISTING OF SPECIAL CHARACTERISTICS

Part Name:                                                                                Part Number:

Customer:                                                 

Preliminary Final
Sr. No.Description of Special CharacteristicsSpecification & TolerancesReason for Spl CharacteristicsControl MechanismRemarks
 ProcessProduct (Refer Notes below)  
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       

Note: Reason for Special Characteristics are Given below:

F/F =Fit / Function;                              

R =Regulatory Requirement                   

E=Environmental 

S=Safety Requirements;                     

CP=Customer Prescribed

These special characteristics must be taken care while formulating PFMEA & Control Plans.

                                                                                                                                                         (Signature)

Example of documentation template for Production Part approval Process (PPAP) in IATF

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Advanced Product Quality Planning (APQP) in IATF. As each business is different, additional documents or revisions would be required to meet your organization’s specific needs, requirements, context, risk profile, etc. ​​If after reading through all of these documents, you feel like you still need a consulting partner to help you develop your new documents – Contact Us. We’re always looking for interesting new clients and projects.

1.0 Process Approach for Production Part approval Process (PPAP)

2.0 Turtle Diagram of Production Part approval Process (PPAP)

Example of Production Part Approval Process of SHAFT COMP., GEAR SHIFT

List of documents submitted

Part Name : SHAFT COMP, GEAR SHIFT                                              Part No. & Rev:                     N8080530  Rev No : L4/d Customer :                                                                                                      Plant Location:   PPAP Submission Level :                                                                             Initial
Sr No.Document TitleApplicable Y/NSubmitted / RetainedRemarks
1List of documents submittedY  
2Design Records Bill Of Material Drawing Test Standards  Y Y N  
3Engineering Change DocumentsN  
4Customer Engineering ApprovalN  
5Design FMEAN  
6Process Flow Diagram Overall Process Flow (for Assembly)  Y  
Process Flow Chart (for Feeder shop & Assembly)
7Process FMEAY  
8Dimensional ResultsY  
9Material Performance Test ResultsY  
10Initial Process Study Control Chart Pp, Ppk Calculation Sheet  Y Y  
11Measurement System Analysis Studies MSA for variable characteristics MSA for attribute characteristics  Y Y  
12Qualified Laboratory DocumentationN  
13Control PlanY  
14PSW Weight Calculation SheetY  
Y
15Appearance Approval ReportN  
16Bulk Material Requirements ChecklistN  
17Sample ProductY  
18Master SampleY  
19Checking AidsY  
20Records of Compliance With Customer-Specific Requirements List of approved TIER 2 suppliers Process Qualification Records   
Y
N

Prepared by:xxxx                                                                                 Date:xx.xx.xxxx

Checked by:xxxx                                                                                          Date:xx.xx.xxxx

Approved by:xxxx                                                                                        Date:xx.xx.xxxx

CONTROL PLAN
 Prototype                   Pre-launch            ProductionKey contact/phone : xxxxDate (Orig.) : xx.xx.xxxxRev No.02/.Date : xx.xx.xxxx
 
Control plan Number :CP/SGS/28
    Part Number/Latest change level : N8080530                   Rev No : L4 / f    Core Team :A,B,C,D,E,F,G,H,I,J    Customer Engineering approval:
Part Name : Shaft Comp, Gear Shift ( Star )Plant approval/ date :Customer Quality approval:
Customer: TVS MOTOR COMPANY LTDOther approval / date (if reqd) :Other approval:
    OPN No.  Process Name/ Operation Description    Machine, device, Jigs & Fixtures for Mfg.CharacteristicsSpec ial Char . Clas sMethods    Reaction Plan
  No .  Product  Process  Product/ Process Specification / ToleranceEvaluation / Measurement Technique  Error proofingSample  Control Method
Size n  Freq.
 
                                                                          0                                                                      Incoming Inspection (Bought out Materials)                                                                        1) Inspection of Shaft, Gear Shift (N8080549)  1  Distance    8.7 -0.15  Height gauge                                                                         As per Receiving Inspection Sampling Plan                                                                        Receiving Inspection Report (QA/FM/01)                                                                    Reject / Segregation / Rework / Send back to supplier
  2  Chamfer    1 x 30°  Visual 
  3  Surface roughness    6.3 Ra  Roughness tester 
  4  Outer dia    Ø10.1 -0.02  Micrometer 
  5  Radius    R0.2/0.4  Visual 
  6  Outer dia    11.5 -0.05  Micrometer 
  7  Outer dia    12e8 (-0.032/-0.059)  Micrometer 
  8  Surface roughness    6.3  Roughness tester 
  9  Surface roughness    1.6 Ra  Roughness tester 
  10  Groove Width    4.2 +0.5  Digital vernier caliper 
  11  Distance    192  VHG 
  12  Distance    183  VHG 
  13  Distance    17.5  VHG 
  14  Groove dia    9.7 -0.25  Digital vernier caliper 
  15  Distance    157.5 +0.15  VHG 
  16  Groove width    1.15 +0.15  Digital vernier caliper 
    OPN No.  Process Name/ Operation Description    Machine, device, Jigs & Fixtures for Mfg.CharacteristicsSpec ial Char . Clas sMethods    Reaction Plan
  No .  Product  Process  Product/ Process Specification / ToleranceEvaluation / Measurement Technique  Error proofingSample  Control Method
Size n  Freq.
 
     17  Radius    R0.2Max  Visual    
  18  Groove dia    11.3 -0.2  Blade micrometer 
  19  Appreance    free from burr  Visual 
  20  Surface treatment    ZnFe Alloy plating  Verify Supplier Report 
  21  Appreance    Free from rust  
  22  Hardness    24±4  Hardness tester 
  23  Distance    2  Digital vernier caliper 
  24  Angle    45°  Bevel protactor 
                                                                        0 Cont.                                                                      Incoming Inspection (Bought out Parts)                                            2) Inspection of ARM (N5080959)  1  Thickness    3.2 +0.1/-0.2  Micrometer                                                                         As per Receiving Inspection Sampling Plan                                                                        Receiving Inspection Report (QA/FM/01)                                                                    Reject / Segregation / Rework / Send back to supplier
  2  Hole dia    7 H9 (+0.036)  Plug gauge 
  3  Height    3.5 ±0.1  VHG 
  4  Hole dia    10.2 ±0.1  Plug gauge 
  5  Distance    95  VHG 
  6  Flatness    0.15 max  VHG / Dial gauge 
  7  CD    107±0.15  Digital vernier caliper 
  8  Position    0.15 WRTB  CMM 
  9  Symmetry    0.15 WRT B  CMM 
  10  Height    12 -0.5  VHG 
  11  Appreance    Free from crack, Dent, burr  Visual 
  12  Case Depth    0.1/0.3  Verify supplier report 
  13  Hardness    80-91 HR15N  Verify supplier report 
  14  Appreance    No buldeg ouward allowed  Visual 
    OPN No.  Process Name/ Operation Description    Machine, device, Jigs & Fixtures for Mfg.CharacteristicsSpec ial Char . Clas sMethods    Reaction Plan
  No .  Product  Process  Product/ Process Specification / ToleranceEvaluation / Measurement Technique  Error proofingSample  Control Method
Size n  Freq.
 
     15  Chamfer    0.5×45°  Visual    
                          3) Inspection of Pawl. ( N8080969 )  1  Distance    4.84 -0.05  CMM 
  2  Angle    35.34 +0.50°/  CMM 
  3  Distance    5 -0.5  CMM 
  4  Distance    61.55 +0.15  CMM 
  5  Distance    37.87 -0.15  CMM 
  6  Hole dia    5 +0.1  Plug gauge 
  7  Flatness    0.2  Dial 
  8  Appreance    Free from crack, Dent, burr  Lever Dial 
  9  HArdness    45 ±3  Hardness tester 
                                        4) Inspection of Rivet (N2080499)  1  Outer dia    Ø8.5 -0.1  Micrometer    
  2  Radius    R0.3 Max  Visual 
  3  Outer dia    Ø7 e9 (-0.025/-0.061)  Micrometer 
  4  Outer dia    Ø5 -0.02/-0.07  Micrometer 
  5  Inner Dia    2.5  Digital vernier caliper 
  6  Surface roughness    N9  Visual 
  7  Depth    2.5  Dial 
  8  Distance    8  VHG 
  9  Distance    3.35 ±0.05  VHG 
  10  Depth    1.5  Digital vernier caliper 
  11  Hardness    78±4  Hardness tester 
  12  Case Depth    0.5/1.0  Supplier Report 
    OPN No.  Process Name/ Operation Description    Machine, device, Jigs & Fixtures for Mfg.CharacteristicsSpec ial Char . Clas sMethods    Reaction Plan
  No .  Product  Process  Product/ Process Specification / ToleranceEvaluation / Measurement Technique  Error proofingSample  Control Method
Size n  Freq.
 
     13  Hardness    247 BHN Max  Supplier Report    
                          5) Insp.of Spacer (N2080970 )  1  Inner Dia    Ø11.58 / Ø11.53  Plug gauge  
  2  Chamfer    0.5 x 45°  Visual 
  3  Outer dia    20.0 -0.15  Micrometer 
  4  Run out    0.05 WRT B  Dial 
  5  Thickness    24.5 -0.15  Micrometer 
  6  Surface roughness    N9  Visual 
  7  Surface roughness    N9  Visual 
  8  ID chamfer    0.3 x 45°  Visual 
  9  Surface roughness    N9  Visual 
                                                                         Welding                                                                        Shaft & Arm Welding   Machine Code:  M/c 1 : W003                              Check Sheet 
  1   Current   150 – 170 Amps  Ammeter   1  Daily  a,b,c
  2   Voltage   22 – 26 Volts  Voltmeter   1  Daily  a,b,c
  3   Gas Flow   15 – 20 LPM  Flow meter   1  Daily  a,b,c
  4 Rotary Welding Speed   H – Full Speed  Stop Watch   1  Daily  a,b,c
  5 Welding Wire Diameter   0.8 mm  Micrometer   1  Daily  a,b,c
  6   Nozzle Cleaning   No Weld Spatters on Nozzle  Visual   Once  Every 5 Piece  a,b,c
  7 Openning the Nozzle & Cleaning   No Weld Spatters on Nozzle  Visual   Once  Every 30 Piece  a,b,c
  8   Liner Cleaning   No Weld Spatters on Nozzle  Visual   Once  Every 1 Week  a,b,c
  9Weld Blow Holes, Incomplete Weld    No Weld Spatters & Incomplete Weld  Visual   100%  Daily        Setup cum In process Inspection Report(QA/FM/0  a,b,c
  10  Rust    Not allowed  Visual   100%  Daily  a,b,c
  11  Knurling Damages    Not allowed  Visual   100%  Daily  a,b,c
    OPN No.  Process Name/ Operation Description    Machine, device, Jigs & Fixtures for Mfg.CharacteristicsSpec ial Char . Clas sMethods    Reaction Plan
  No .  Product  Process  Product/ Process Specification / ToleranceEvaluation / Measurement Technique  Error proofingSample  Control Method
Size n  Freq.
 
10Shaft & ARMMachine : W003  12  Groove Pressence    Not allowed  Visual   100%  Daily2) & Gauge Frequency check sheet(QA/FM/14) .  a,b,c
  13  Bush Float    Not allowed  Visual   100%  Daily  a,b,c
  14  Arm Flatness    Not allowed  Visual   100%  Daily  a,b,c
  15  Arm Height    18.2 + 0.2  Position Gauge / VHG                   Setup approval first 5 nos Inprocess 1 no / every 2 hrs by QA (Inspector), Gauge frequency check 5 nos/ every one hour by Operator & also by Final Inspector.                  Setup cum In process Inspection Report(QA/FM/0 2) & Gauge Frequency check sheet(QA/FM/14) .  a,b,c,d
  16  Perpendicularity    0.25 WRT F  CMM   a,b,c,d
  17  Arm to Shaft Height    5.5 ± 0.2  Position Gauge / VHG  
  18  Welding fillet    3mm  Digital vernier caliper   a,b,c,d
  19  Serration angle    5° ± 1°  CMM/ Position gauge   a,b,c,d
  20  Welding strength    >150 NM  UTM / once in a month   a,b,c,d
  21  Spacer rotation    Free Movement  Manual  
              20              Riveting            Riveting Machine : RM002  1   Air Pressure   5 – 6 Bar  Pressure Gauge   1  Daily  Check Sheet  a,b,c
  2   Pawl Bend & Twist   Pawl to be Freely Entry to Acc. Gauge  Acceptance Gauge   100%  DailySetup cum In process Inspection Report(QA/FM/0 2) & Gauge Frequency check sheet(QA/FM/14) .  a,b,c
  3   Pawl Free Rotation   Pawl to Freely Rotate on Axis  Visual   100%  Daily  a,b,c
    4     Pawl Float     Not allowed    Visual     100%    Daily    a,b,c
     I  Appearance  Inspection    Visual    
    1    Damages, Rust, Burr      Not allowed    Visual       a,b,d,e
  2Wrong parts,Child Parts & Operations Missed    Not allowed  Visual   a,b,d,e
  3  Dent    Not allowed  Visual   a,b,d,e
    OPN No.  Process Name/ Operation Description    Machine, device, Jigs & Fixtures for Mfg.CharacteristicsSpec ial Char . Clas sMethods    Reaction Plan
  No .  Product  Process  Product/ Process Specification / ToleranceEvaluation / Measurement Technique  Error proofingSample  Control Method
Size n  Freq.
 
        30        Final Inspection      Inspection Area with Measuring Instruments and Gauges  4  Weld spatters    Not allowed  Visual           As per sampling plan (QA/FM/03)        Final Inspection report (QA/FM/05)  a,b,d,e
  5  Rotation of Pawl    Free Rotation  Manual  
  6  Sharp corners    Not allowed  Visual   a,b,d,e
  II  DIMENSIONAL  INSPECTION      
  1  Perpendicularity    0.25 WRT F  CMM   a,b,d,e
  2  Symmetry    0.15 WRT  CMM   a,b,d,e
  3  Rivet Height    1.3 (ref)  Digital vernier caliper   a,b,d,e
  4  Serration angle    5°±1°  CMM   a,b,d,e
    40  Layout Inspection  Inspection Area with Measuring Instruments and Gauges  As per drawing Dimensions to be checked, as per layout inspection plan – Layout Inspection report.(QA/FM/12 / QA/FM/13)    a,b,d,e
  50  Dispatch  Dedicated crates – 16 Nos / Crate ( Photo attached )
  a – Stop Production,  b – Notify Supervisor,  c – Re-adjustment,  d – Segregate previous batch,  e – Quarantine non-conforming parts,  f – Tool Rectification
  Prepared By :Mohan raj         Approved By : Ashokkumar  
  Revision History
  Sl.no  Rev.No  Date  Details of Revision  Revised by
  1  01  xx.xx.xxxx  Inspection Details with Qty  xxxx
  2  02  xx.xx.xxxx  Dimension 5.5 ± 0.2 Parameter Added and also Gauge Inspection Added in Final Inspection Stage  xxxx

FINAL INSPECTION REPORT

VENDOR CODE : 20686VENDOR NAME :
CUSTOMER :Part No : N8080530                        Rev No : L4 / dPart Name : Shaft comp Gear shift
Invoice No :Date :Lot Size :Sample Size:
SL. #PARAMETERSSpecial Char. ClassSpecificationMethod of InspectionOBSERVATION BY TAL  Cp  CpKOBSERVATION AT TVS M
12345678910
IAPPEARANCE  INSPECTION   
  1  Damages, Rust, Burr   Not allowed  Visual             
  2Wrong parts,Child Parts & Operations Missed   Not allowed  Visual             
3Dent Not allowedVisual             
4No Weld spatters Shall presentVisual             
  5  Sharp corners   Not allowed  Visual             
IIDIMENSIONAL  INSPECTION    
1Perpendicularity yes0.25 WRT FCMM             
2Symmetry yes0.15 WRT FCMM             
3Rivet Height 1.3 RefVHG             
4Serration angle 5°±1°CMM/Position Gauge             
INSPECTED BY: Sign. / xxxxVerified at TVS Sign. / Dt.If RW/SG Job Order No:LAB / ETR NO:Acceptance Status DP / RW / SG / RJGRN NO: DATE:
For previous lot Rejection / RT/Segregation & Field failure parameters check double the Sampling Quantity.Sampling PlanLot Size0 – 50                  51 – 100                101 – 500                     501 – 2000            > 2000
Sample sizeAppearance/Dimensional3                             5                            10                               20                          40
Performance1                             1                             1                               2                             3

Product Weight Details

Part Name: Shaft comp gear shift                           Part No. & Rev : N8080530 Rev No :L4 /d Customer :                                                                         Plant Location : xxxx
Sr No.Weight in Kgs (upto 3 decimels)Remarks
  1  0.32 
  2  0.300 
  3  0.33 
  4  0.310 
  5  0.3 
  6  0.320 
  7  0.32 
  8  0.3 
  9  0.32 
  10  0.310 
Average0.313kg

Prepared by:xxxx                                                            Date.xx.xx.xxxx

Checked by.:xxxx                                                            Date.xx.xx.xxxx

Approved by.:xxxx                                                          Date.xx.xx.xxxx

List of Checking Aid

  Part Name : SHAFT COMP. GEAR SHIFT    Part No. & Rev:N800530& L4 / d
Customer Name :   Plant Location: 
  Sr No.  Characteristics / Specification / RequirementChecking Aid used (Attr/Var)  Checking Aid NameChecking Aid NumberCalibration Due Date  R&R details  Remarks
1Perpendicularity0.25 WRT FVCMMCMM-01xx.xx.xxxx  
2Symmetry0.15 WRT FVCMMCMM-01xx.xx.xxxx  
3Rivet Height1.3 RefVVHG – Dial ind.counter type with Hy.MandrelQA/VHG/01xx.xx.xxxx  
4Serration angle5°±1°ACMMCMM-01xx.xx.xxxx  

Prepared by: xxxx                                Date :xx.xx.xxxx

Checked by: xxxx                                 Date : xx.xx.xxxx

Approved by: xxxx                                Datexx.xx.xxxx

                                                                                                                                                      
                       Customer Specific Requirements
Annexure-07
Rev 01   dated -01.12.2020
Customer Spectific Requirement Matrix
IATF RequirementsCustomer specific additional Requirements for TVS Motor  ( ref. SQAM Supplier Quality Assurance Manual )Customer specific additional Requirements for MultimaticCustomer specific additional Requirements for Jay IndustriesCustomer specific additional Requirements for Lander AutomotivesCustomer specific additional Requirements for JostCustomer specific additional Requirements for Rockman IndustriesCustomer specific additional Requirements for Diado IndiaProcess Name
 (Where this requirement is applicable)
4.1No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
4.2No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
4.3No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
4.4No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
5.1No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
5.2No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
5.3
Organizational roles, responsibilities and authorities
The supplier shall submit an organisation chart including the roles and responsibilities of each function and number of persons (Manager, Executives, and Inspectors) along with the contact information.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsHR
The supplier shall notify TVSM of any changes in their contact information as and when they are made. Revised forms shall be sent within 7 days of such changes.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
6.1No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
6.2No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
6.3No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
7.1.5.1.1
Measurement systems analysis
Supplier shall use MSA reference manual latest edition of AIAG for all attribute and variable gauge studies.Supplier shall use MSA reference manual latest edition of AIAG for all attribute and variable gauge studies.Supplier shall use MSA reference manual latest edition of AIAG for all attribute and variable gauge studies.Supplier shall use MSA reference manual latest edition of AIAG for all attribute and variable gauge studies.Supplier shall use MSA reference manual latest edition of AIAG for all attribute and variable gauge studies.Supplier shall use MSA reference manual latest edition of AIAG for all attribute and variable gauge studies.Supplier shall use MSA reference manual latest edition of AIAG for all attribute and variable gauge studies.Quality
On an on going basis, the supplier shall conduct Gauge R&R (variable and attribute studies) on all types of measurement systems at least once in a year
The types of measurement system shall be identified / grouped based on instrument type, instrument range and resolution, part characteristics, operating environment and skills / competences of personnel using the instrument.
7.2No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
7.3No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
7.4No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
7.5
Documented information
Retention period- 2 Years
Inspection Standards, Inspection Reports, Tooling Maintenance Reports, Control Chart, Material Test Reports, Performance Test Reports, Calibration Records, Machine Capability Study Reports, Audit Reports, QUALITY DEVIATION HIGHLIGHTS, Action Plans, Kaizens, QC Story
No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsControl of documented information
Retention period- Life of the product
Drawings, APQP Documents and Master Samples
Retention period- Life of the product
Drawings, APQP Documents and Master Samples
Retention period- Life of the product
Drawings, APQP Documents and Master Samples
Retention period- Life of the product
Drawings, APQP Documents and Master Samples
Retention period- Life of the product
Drawings, APQP Documents and Master Samples
Retention period- Life of the product
Drawings, APQP Documents and Master Samples
Retention period- Life of the product
Drawings, APQP Documents and Master Samples
8.1No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements 
8.2.3.1.3
Organization manufacturing feasibility
Prepare Manufacturing Feasibility and Risk Analysis format QSF PUR SQAM 002,003 and drawing feedback & agreement form QSF PRG 02 01 018 and feedback / suggestions for QCD improvementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsMarketing & Sale and New Product Development
manufacturing feasibility as per checklist QSF PUR SQAM 003No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
Supplier shall use TVSM format QSF QAD 10 11 05 for preparation of AOINo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
8.3.2
Design and development planning
Readiness Review– This is done by reviewing product and process design documents as per checklist CL QAD 10 11 001No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNew Product Development
IPTR (Initial Production Trial Run)– typically 50 nos. and reviewing the results as per checklist CL QAD 10 11 002No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
SPTR (Significant Production Trial Run)– (8 hours Production or 300 nos ) at planned run-at-rate and reviewing the results as per checklist CL QAD 10 11 003No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
8.3.3.3
Special characteristics
Safety / Statutory / regulatory- severity = 9 or 10.
 Minimum Process Performance index / process capability levels for variable characteristics 1.0 for geometric & 1.67 others
Follow as per DrawingFollow as per DrawingFollow as per DrawingFollow as per DrawingFollow as per DrawingFollow as per DrawingNew Product Development
Fit / Function – Critical- severity = 7 or 8.
Minimum Process Performance index / process capability levels for variable characteristics 1.0 for geometric & 1.67 others
Fit / Function – major- severity = 5 or 6.
Minimum Process Performance index / process capability levels for variable characteristics 1.0 for geometric & 1.33 others
Supplier shall send the of process capability reports on monthly basis for special characteristics, controlled through X-bar, R chart. Action plan to be submitted to improve the process capability, if Cpk is below the norms specified in the manual.Quality & Production
8.3.4.4
Product approval process
Submit the PPAP documents through Collaboration Folder link available on http://www.tradewithtvs.com and Table 1 shows the 19 requirements for the PPAP submissionPilot Lot of 300 nos along with PPAP Documents
Material reports to be uploaded on IMDS If required
Intial 10 nos  nos along with PPAP DocumentsIntial 5 nos  nos along with PPAP Documents
Material reports to be uploaded on IMDS if required
Intial 05 nos  nos along with PPAP DocumentsIntial 10 nos  nos along with PPAP DocumentsIntial 10 nos  nos along with PPAP DocumentsNew Product Development
8.3.5.2
Manufacturing process design output
FMEA shall follow the latest edition of FMEA reference manual published by AIAGNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNew Product Development
High risk in FMEA is defined where severity is high and / or RPN is high for a failure mode / cause. High Severity ³ 7 or High RPN ³ 63 ( action plan required to reduce severity or RPN ).No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
special attention to be given for high severity rankings even if RPN is low. Whenever severity is 9 or 10 and no actions are possible to reduce severity ranking, efforts shall be taken to minimize occurrence and detection ranking.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
8.4
Control of externally provided processes, products and services
Maintain master list of all the T2 suppliers with clear details of the operations carried out and provide a copy to TVSM along with PPAP.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsPurchase & Quality
Carry out special processes like heat treatment, plating, painting, powder coating etc only at the mutually approved sources.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
TVSM may review the PFD, PFMEA & Control Plan of the Tier 2 supplier during part development if required.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
8.4.2.4.1
Second Party Audit
Supplier shall make a plan for Tier 2 audit covering all Tier2 suppliers.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsPurchase, G.M Systems & Quality
Supplier shall verify following areas
– Availability of latest revision of drawing and inspection standard
– Adherence to Control Plan
– Condition & Calibration of Gauges / Instruments / Tool / Equipments
– Part parameter audit
– Condition of jig / fixture / tools / gauges & history maintenance.
– NC products identification and handling
– Deployment of certified operators and inspectors in critical processes
– If a special process is done by Tier 2, then the special process qualification to be verified and approval by TVSM.
– Layout inspection, product audits.
– Supplier may cover additional areas as required
No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
8.5.1
Control of production and service provision
Process Qualification
Supplier shall identify the special processes ie (Heat treatment, Plating, Painting, Powder Coating, Welding, etc) and make a plan for conducting the process qualification, including Tier 2.
No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsQuality, Production & Purchase
The process shall be set at minimum condition for all process parameters as per the Control Plan and produce the product as per the normal batch size. (E.g. Temp: 160 ~ 200 deg Time: 5minutes ~ 8 minutes in a plating process then produce the batch by setting temp at 160 deg and time 5 minutes for minimum condition)No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
8.5.2.1
Identification & Traceability
Batch Number
Supplier Identification
LH / RH designation
Date of manufacture, Month, Year
Cavity no, Mould no, Die no,
Date Code / Heat Code
No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsProduction, New Product Development & Tool Management
8.5.1.6
Management of production tooling and manufacturing, test, inspection
tooling and equipment
Issue Tool Ownership Certificate (QSF PUR SQAM 017) to TVSM, once the tools are proved.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsTool Management
Review the condition of tool when quantity produced reaches 75 % of the agreed life. Thereafter, review the tool condition at incremental 10% production of the agreed tool life quantityNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
8.5.6.1
Control of changes
Supplier shall submit request for engineering changes – format no. QSF PUR SQAM 014, process changes format no, QSF PUR SQAM 013 and obtain necessary clearance from TVSM for going ahead with the change implementation.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNPD
8.6No additional requirementsMaterial TC and Inspection report with each every dispatchMaterial TC and Inspection report with each every dispatchNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
8.7.1.1
Customer authorization for concession
Non-conformance of Minor in nature
If the non conformance is minor in nature and if the supplier feels that it will not affect either the subsequent process at TVSM or the intended functional requirements at TVSM customer’s end, then they shall request TVSM for clearance thro, Deviation Approval Request format (QSF PUR SQAM 007) immediately and explain the non conformance nature.
No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsQuality
The suppliers are notified through Quality Deviation Highlights (QDH) on Web http://www.tradewithtvs.com, the supplier shall ensure corrective actions on receipt of QDH and communicate the causes of failure.
QDH raised for non-conformance shall be replied within 24 hours through E-Mail, Fax, Courier, or in person.
No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements 
8.7.1.6
Customer notification
Non-conforming parts shipped to TVSM and suppler end
Supplier shall send Notification of Suspected Shipment of Non-confirming Product format (QSF PUR SQAM 006) to TVSM Purchase / Quality
No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsQuality
9.1.1.1
Monitoring and measurement of manufacturing processes
SPC shall be in line with latest edition of AIAG manualNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsQuality & Production
Process capability studies shall be carried out over a sample size of minimum 100 nos. (25 subgroups of 4 samples each or 20 subgroups of 5 samples each)No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
If the process becomes unstable or non-capable (as per table), supplier shall introduce 100% inspection for the parameter, till the Corrective Action is taken and normalcy restored.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
Supplier shall send the of process capability reports on monthly basis for special characteristics, controlled through X-bar, R chart. Action plan to be submitted to improve the process capability, if Cpk is below the norms specified in the manual.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirements
9.1.2.1
Customer satisfaction
Quality performance report for each supplier is published on the website http://www.tradewithtvs.com. Quality rating is arrived based on the quality performance covering lot, line rejections, and warranty returns including spare parts supply. If rating is less than 90%, supplier shall forward the action plans proposed / planned along with the time frame to meet the target, the progress of which shall be reviewed by the supplier management on monthly basis and to be presented to TVSM on demand.No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsQuality, Marketing & Sale
9.2.2.4
Product Audit
Supplier shall perform product audit for ready for despatch parts, to confirm dimensions against standard, Functionality, Packaging, Labeling, etcNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsPurchase & Quality
9.3No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
10.1No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA
10.2.5
Warranty management systems
Analyze the failure, using warranty analysis guidelines and warranty analysis summary format QSF PUR SQAM 010 & QSF PUR SQAM 011. It is recommended to check 50 – 100 nos of failed parts randomly and verify the following observations.
– Phenomena of failure, kms etc
– Location of failure
– Bench mark study to identify the improvements
– Simulation of field failure in lab
– Identify the root cause of failure
– Identify the counter measure
– Compare the improvement in lab testing (before & after)
– Implement the action with time plan format
– Monitor the results
No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsQuality, Marketing & Sale
The implemented corrective action score shall be minimum 4
Detection type
Poka Yoke
• Design improvement
(Sev 5 to 7)
• Process improvement
(Cpk 1.33 to1.67)
• 100% additional
test station
• Automation of tool
change frequency
– visual control
No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsQuality
10.2.6
Customer complaints and field failure test analysis
Upon the receipt of complaint (Email / Fax / Quality Deviation Highlights), supplier representative shall visit TVSM to understand the problem within 24 hours.Corrective action required to submit on DMN PortalNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsQuality
M1 action – Immediate action to be taken on stocks at TVSM- Quarantining / segregation / 100% inspection etc.
Target lead time for completion of M1 action -Within 24 hrs
M2 action -Temporary action to be taken at all stages of manufacturing, transit and storage through out the supply chain. to prevent the defect reaching TVSM.Example of means used –100% inspection / switch over from sampling to 100% inspection / Gauge introduction, etc
Target lead-time for completion of M2 action – Within 48 hrs
M3 action – Corrective action through problem solving approach (QC Story/Kaizen sheet/8D- report )
Target lead-time for( i) Submission of corrective action reports –within 7 days
(ii) completion of M3 action – Within 15 days (according to the nature of problem and resolution)
10.3No additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNo additional requirementsNA

Example of documentation template for Control of drawing including ECN and ECR in IATF

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Control of drawing including Engineering change note (ECN) and Engineering change Request(ECR) in IATF. As each business is different, additional documents or revisions would be required to meet your organization’s specific needs, requirements, context, risk profile, etc. ​​If after reading through all of these documents, you feel like you still need a consulting partner to help you develop your new documents – Contact Us. We’re always looking for interesting new clients and projects.

1.0 Process Approach For Drawing Control , ECN and ECR

2) Turtle Diagram For Drawing Control , ECN and ECR

3) Engineering Change Request

  Engineering Change Request
    Part Name :    Date:
  Part Number/Drg Number :  Deptt: Name ;-
  Request to Dept.Name 
  S.No.  Existing Dimensions/Part  Changes Required  Reasons of changes  Remark If any
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
  REQUESTED BY    APPROVED BY

4) Engineering change Note

5.0 Drawing Tracker sheet

Example of documentation template for Advanced Product Quality Planning (APQP) in IATF

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Advanced Product Quality Planning (APQP) in IATF. As each business is different, additional documents or revisions would be required to meet your organization’s specific needs, requirements, context, risk profile, etc. ​​If after reading through all of these documents, you feel like you still need a consulting partner to help you develop your new documents – Contact Us. We’re always looking for interesting new clients and projects.

1.0 Process Approach for Advanced Product Quality Planning (APQP)

2.0 Turtle Diagram for Advanced Product Quality Planning (APQP)

3.0 AQP Timing Plan Macro Level

Project Name :                 Project No : Project Leader :
 Description PlannedActualRemarks
1CFT Sign OffTeam Leader & CFT   
2Availibility  of Ref sample /3d model    
3Feasibility reviewTeam Leader & CFT   
4Drawings finalize on TAL FormatTeam Leader & Engg. HOD   
5Lsit of Discrepenceies observed in drgs.Team Leader & Engg. HOD   
6Share Observations with Customer & Ask for Clarifications   5- samples along with Insp. Report to be submit to customer 25th Dec.2015
 Submiited for ClearanceProcess owner   
 Signed for clearance of Gate -1Engg HOD   
 Signed for clearance of Gate -1DGM-   
1BOM /List of Raw material – In – ERP    
2Verification of Material TC from NABL Approved LabQuality   
3Fit & Finish Requirements & Agreement on Specimen / level with customerTeam Leader / Engg. Head & Customer  5- samples to be submit to customer 25th Dec.2015
4Completion of Preliminary PFD /FMEA/CPTeam Leader  & CFT   
5List OF Tools , Gauges & Jig fixturesTeam Leader  & CFT   
6Closer of all Clarifications & Sign offCustomer SQA  / Team Leader  Will be close after getting feed back of Customer
7Tools, Fixture & Jig Designing (Tooling concepts to be Review & finalize in CFT )Team leader /CFT   
8Gauges Designing (Concepts to be Review & finalize in CFT) (Final check fixture & in process gauges)Team leader /CFT   
9Validation of Tools, Jig & Fixture Design ( w.r.t. FMEA )Engg HOD / CFT   
10Validation of Gauge Designs (Final check fixture & in process gauges)Engg HOD / CFT   
 Submiited for ClearanceProcess owner   
 Signed for clearance of Gate -2Engg HOD   
 Signed for clearance of Gate -2DGM-   
1Tools, Jig & Fixture ManufacturingTool Room   
2Tools, Jig & Fixture Inspection ( Assy. & Stage inspection)Tool Room   
3Tools, Jig & Fixture Issue to ProductionTool Room / Process Owner   
4Gauges ManufacturingTool Room   
5Gauges Inspection -Tool room ( Assy. & Stage inspection)Tool Room   
6Gauges Calibration -Standard RoomQuality   
7Floor plan Layout approved by DirectorsTeam leader   
8New / Existing Machines/Equipment RequirementTeam leader /CFT   
9Tool Trial report with 10 no’s of samplesTool Room   
1010 no’s child parts hand over to Std Room for layout with inspection reportProcess Owner / Quality   
11Approved Samples along with Signed ISIR Document -Send to CustomerQuality /Team Leader   
12Fitment Trials at Customer End    
      

4.0 TEAM FEASIBILITY COMMITMENT

 Date:

Part Name:                                                                                            Part Number :

 Customer :                                                                                           Vehicle / Model:

  Feasibility Consideration:

 CFT has considered the following questions, not intended to be all-inclusive in performing a feasibility evaluation. The drawings and / or specifications provided have been used as a basis for analyzing the ability to meet all specified requirements. All “NO” answers are supported with attached comments  identifying comments and / or proposed changes to enable us to meet the specified requirements.      

YESNOCONSIDERAION
  Is product adequately defined (application requirements etc.) to enable feasibility review?
  Can Engineering Specification be met as written?
  Can product be manufactured to tolerances specified on drawing?
  Can Product be manufactured with Cpks’ that meet requirements?
  Is there adequate capacity to make the product?
  Does the design allow the use of efficient materials handling techniques?
 Can the product be manufactured without incurring any unusual :
  Cost for Capital Equipment?
  Cost for Tooling?
  Alternative Manufacturing Methods?
  Is Statistical Process Control required on product?
  Is Statistical Process Control presently used on similar products?
 Where Statistical Process Control is used on similar products :
  Are the processes in control and stable?
  Are Cpk’s greater than 1.33?

     CONCLUSION :

 FeasibleProduct can be produced as specified with no revisions
 FeasibleChanges Recommended (See Attached Comments)
 Not FeasibleDesign Revision required to produce product with in specified requirements
     Comments:  _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __ _ _ _ _ _ _ _  _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __ _ _ _ _ _ _ _    _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __ _ _ _ _ _ _ _

    SIGN-OFF

  Team Member/Title/Date  Team Member/Title/Date                  Team Member/Title/Date

   Team Member/Title/Date            Team Member/Title/Date            Team Member/Title/Date

SUPPLIER SIGN-OFF

Supplier Name/Date                       Supplier Name/Date                         Supplier Name/Date

5.0 APQP Cross Functional Team

Date:  

Product:                                                                         Part No.:                                        

Customer:

Scope of Team:

Team Leader:                                                               Position:

Team Members:

Sr. No.NameDeptt.DesignationMajor ResponsibilitySignature
01     
02     
03     
04     
05     
06     
07     
08     
09     
      

Meeting Frequency:

Team Leader:                                                                         Date:

6.0 Customer Specific Requirements

    S. No.    Name of Customer    Part #    PPAP Level  APQP Timing Plan  Special Characteristics of Products  Delivery InstructionsPre Dispatch Inspection Report    Packaging standard  Record Retention Period  MSA Plan  SPC (Cpk)  Callibration Lab ApprovalCustomer Approved Supplier (If any)  Inspection Standards (If any)  Ref. Standard  Proto type Samples sizeLine Rejection at Customer end from other supplier    Remarks
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   

7.0 Listing of Special Characteristics

LISTING OF SPECIAL CHARACTERISTICS

Part Name:                                                                                                        Part Number:

Customer:                                                 

Preliminary 
Final 
Sr. No.Description of Special CharacteristicsSpecification & TolerancesReason for Spl CharacteristicsControl MechanismRemarks
 ProcessProduct (Refer Notes below)  
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       

Note: Reason for Special Characteristics are Given below:

F/F =Fit / Function;                              

R =Regulatory Requirement                   

E=Environmental

S=Safety Requirements;                     

CP=Customer Prescribed

  These special characteristics must be taken care while formulating PFMEA & Control Plans.

                                                                                                                                                         (Signature)

8.0 Identification of New Machine

IDENTIFICATION OF NEW MACHINES/  EQUIPMENTS
1. Identify significant characteristics (a) Product b)Process (Machining / Heat treatment /Welding / Surface protection) c) EEC parameters etc.
S.No.CharacteristicsOperation (Stage)Control  Mechanism
    
    
2. Fit & Finish Requirements & Agreement on Specimen /Level
Aesthetics: Agreement on Surface finish, Appearance ,Abnormalities and Assy related like Gap,Mismatch,Eveness and eccentric etc
Reference Sample Sign Off
Revalidation  Frequency
3. Tooling  – Cutting tools &  jigs and fixtures
S.No.Tooling  RequirementMakeQuantityCompletion date
     
     
4. New / Existing Machines / Equipment requirement
S.No.Machine / EquipmentMake / TypeAvailability Status
    
    
5. Material Handling Equipment Requirement
S.No.EquipmentMakeQuantityCompletion date
     
     
6. Supplier selection for Bought-out Parts
S.No.PartsSupplier NameTVS to approve (Yes / NO)
    
    
7. Sub-contracting requirements
S.No.Operation NameSupplier NameTVS to approve (Yes / NO)
    
    
8.Gauges/Instruments / Test Equipment requirements
S.No.Gauges / Instruments / Test Equipment DescriptionMakeQuantityCompletion date
     
     
9. Identification & Traceability
MethodStamp
Supplier  identificationTAL & IR No.
LocationHing, Rear Brake
TraceabilityTAL & IR No.
10.Packing Method agreement-Explain the method briefly
Part preparation (Cleaning and oil application etc.):                                   
Method of Primary packing:
Method of Secondary packing:.
Type of strapping:

9.0 PROCESS FAILURE MODE AND EFFECT ANALYSIS (PROCESS FMEA)

Item :Process Responsibility :FMEA Number :
Core Team :Key Date :Prepared By :
Part No./Latest Change Level: FMEA Date(ORG) :Rev :
ModelYear  (S)/Program(S)Customer:-
  OPN No.  Process Function/ Requirement    Potential Failure Mode    Potential Effect(s) of Failure    Sev.    ClassPotential Cause(s) Mechanism(s) of FailureCurrent Process Controls    RPN  Recommended Action(s)  Resp. & Target, Completion DateAction Results
Controls Prevention  Occ.Controls Detection  Det.Actions Taken Completion Date    Sev    Occ    Det    RPN
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
  Prepared By:                                                                                                                                                                                                                                                                                                                                                                    Approved By:

10) Control Plan

Customer:-   Customer code:-Other Approval  /Date (if Reqd.) Other Approval / Date:- 
   Characteristics Methods 
 Process Name/Machine,Device,No.ProductProcessSpecialProduct/ProcessEvaluationSamplesControl MethodReaction Plan
Part/ProcessOperationJig,Tools   Char.Specification/MeasurementSize nFreq.  
NumberDescriptionFor  Mfg.   ClassTolerancesTechnique  
             
             
             
             
             
             
             
             
             
             
a – Stop Production,   b – Notify Supervisor,   c – Re-adjustment,   d – Seggregate previous batch,   e – Quarantine non-conforming parts,   f – Tool Rectification    
 Prepared by :-        
Approved by :  
Revision History    

11) Process flow diagram

Part Name  :   Customer:-   Revision :
Part No./Latest Change Level:      PPD BY :
OPN No.FabricateMoveStoreInspect  Operation DescriptionItem No.Key product / process characteristics  Key Control Characteristics
    productProcess
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          
          

12) Floor Plan Check list

CUSTOMER OR INTERNAL PART NO. :-

QUESTIONYESNOCOMMENT/
ACTION REQUIRED
PERSON RESPONSIBLEDUE DATE
1Does the floor plan identify all required process and inspection points?Yes    
2Have clearly marked areas for all material, tools, and equipment at each operation been considered?Yes    
3Has sufficient space been allocated for all equipment?Yes    
           Are process and inspection areas: 
4Of adequate size?Yes    
5Properly lighted?Yes    
6Do inspection areas contain necessary equipment and files?Yes    
           Are there adequate:  
7Staging areas?Yes    
8Impound areas?Yes    
9Are inspection points logically located to prevent shipment of nonconforming products?Yes    
10Have controls been established to eliminate the potential for an operation, including outside processing, to contaminate or mix similar products?Yes    
11Is material protected from overhead or air handling systems contamination?Yes    
12Have final audit facilities been provided?Yes    
13Are controls adequate to prevent movement of nonconforming incoming material to storage or point of use?Yes    

13.0 Measurement System Analysis(MSA) Plan / Study Results

Part Name:                                                                        

Part Number:

Customer:                                                                                                                                                       

S.No.Instrument & ID No.RangeResolution (Least Count)CharacteristicsSpec of PartReason for MSA*Type of analysisObserved ResultsAction, if any
       R&RBias/ LinearityR&RBias/ Linearity 
            
            
            
            
            
            
            
            
            
            
            

14.0 PpK and CpK PLAN / STUDY RESULTS

        Part Name:                                                                                              Part Number:

        Customer:   

Sr. NoProduct CharacteristicsReason for IdentifyingStage & M/C (Operation)Results of Cpk / Ppk StudyAction, if any
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      

 NOTE: Refer FMEA/Control Plan and ensure that for all Special Characteristics, Ppk must be identified.

1)  Ppk / Cpk are applicable only for such operations which are stable.

2)  For unstable processes, 100 % inspection is carried out.

                                                                                                                                                                                                                                                                                          Signature                                                                                                                              

14.0 PRODUCT / PROCESS QUALITY SYSTEM REVIEW

 Part Name:                                                                                                Part Number:

 Customer:                                                                                     

SR NoExpected ModificationsRequired Yes / NoIf Yes, Action ReqdResponsibilityRemarks
1Any Change in Documentation :   – Manual – Procedures – Work Instruction – Control Plan – Inspection Std. – Process Control  Sheet      
2.Changes in the Materials Storage Systems    
3.Change in the Inventory Norms    
4.Change in the Material Handling Systems    
5.Any Training required for new instruments being taken    
6.Any Modification in the existing processes    
7.Additional SPC tools to be used    
8.Mistake Proofing required, if any    
9.Change in Plant Layout    
10.Any Change in the Purchasing System    
11.New Vendors to be developed    
12.Modifications in the  Internal Audit Schedule    
13.      Any other not referred above:      

                                                                                                 (Signature)

15 Process Sign Off Sheet

SUPPLIER: PROGRAM:  
MFG LOCATION:CHANGE LEVEL (S):  
PART NUMBER (S):PRE-PSO MEETING DATE
PART NAME (S):ISO CERT. #         TS CERTIFICTE #   ISO 14001CERT. #  

EXPIRATION DATE:  
EARLY CONTAINMENT REVIEWED      YES                 NO      
PSO PROCESS ELEMENTS VERIFIEDDOCUMENTATIONPROCESS
 ACCEPT UNACCEPT ACCEPT UNACCEPT
1PART NUMBER, DESCRIPTION AND CHANGE LEVEL        
2PROCESS FLOW DIAGRAM AND MANUFACTURING FLOOR PLAN    
3PROCES FMEA    
4ERROR AND MISTAKE PROOFING COMPLETE    
5PROBLEM SOLVING METHODS 8-D & 5-WHY    
6INCOMING AND OUTGOING MATERIAL QUALIF/CERT    
7TEST SAMPLE SIZES AND FREQUENCIES    
8PARTS PACKAGING AND SHIPPING SPECIFICATION    
9PARTS HANDLING PLAN    
10ENGINEERING STANDARDS IDENTIFIED    
11PREVENTIVE MAINTENANCE PLANS    
12GAUGE AND TEST EQUIPMENT EVALUATION    
13TOOLING, EQUIPMENT AND GAUGES IDENTIFIED    
14SPECIAL PRODUCT AND PROCESS CHARACTERISTICS IDENTIFIED    
15CONTROL PLAN    
16EVIDENCE OF PRODUCT SPECIFICATIONS    
17PROCESS MONITORING AND OPERATOR INSTRUCTION    
18LINE SPEED DEMONSTRATION    
19INTERNAL AUDIT    
20CUSTOMER SPECIFIC    
CORRECTIVE ACTION REQUIRED YESPROMISE DATE:
 NO
 
ALL PROCESS SIGN – OFF ELEMENTS APPROVED ?                 YES   NO  
PROCESS SIGN OFF TEAM    

TITLE                                        PRINT NAME & SIGN                                                         


TITLE                                         PRINT NAME & SIGN


TITLE                                         PRINT NAME & SIGN
  ALL CORRECTIVE ACTIONS ARISING FROM THIS PSO SHALL BE SUBMITTED TO THE CUSTOMER WITHIN THE PROMISE DATE SHOWN ON THIS FORM.

16) Bill of Materials

 Doc No :
Part No :                                                Drg.Rev.No : Part Name : Customer Name :Rev No :               Date:
Page No : 1 of 1
Control status :
BILL OF MATERIALS
  Sl.No  PART NO  DESCRIPTION  LEVELDrg.Rev. Status  Supplier  No.Off  units
        
        
        
        
        
        
        
        
        
        
        
        
        
      Prepared By :                                                                                                                      Approved By :

17) Part Submission Warrent

18) BENCH MARK DATA / PRODUCT – PROCESS ASSUMPTION

Part Name:                                                    Part Number:    

Customer:                                                     Person Contacted/ Interviewed, if any                                                                                                                        

Date of Visit:

A. Bench Marking Data

S. No.Bench Marking CriteriaBench Marking DataCompany’s Data (Similar Product)
  Supplier (Competitor)ProductDataCurrent StatusAssumed Target
1.1Specific Applicable Features Requiring Attention :     
a)Productivity     
b)Cost / Unit     
c)Cost of Consumption of Consumables Per Unit     
d)Delivery Performance %     
e)Customer Satisfaction Index     
f)Plant Rejections %     
g)Re-works %     
h)Customer Returns     
i)Warranty Claims (ppm)     
j)Others (Specify)               

B. Product / Process Assumptions

2.1Specific Assumptions Related to Product Under Development: TechnologyMaterialsOperational Control / Features
2.2The process of Bench Marking Partner (other supplier) and if the company needs the technological modification / acquisition.  
2.3Special Features of the process, (if Company does not have it).  
2.4Source of Acquisition if the Technology is new.  

Note : For Company’s Assumed Targets, make Action Plan (after feasibility is over) for achieving     or exceeding the Bench Marking Data.

                                                  (SIGNATURES)

19) CHECK LIST FOR RELIABILITY & QUALITY GOALS

   Part Name         :                                                                                   Part Number      :

   Customer          :                                                                                   Vehicle / Model:

A. Reliability Goals

S.NoReliability & SafetyRequirements
  Normal ConditionsAbnormal Conditions
a.Expected Life of development Product under different operating conditions    
b.Safety Features (If any)     

 ote: Use Bench Marking Data if any.

B ) QUALITY  GOALS

(Make Action Plans for Achieving Targets)

Rejection at:                           Current Data               Bench Marking            Assumed Target

(Ppm / %)                                 Similar (Product)            (If any)                      

Customer End:                           ——————         ——————     ——————

End User           :                       ——————          ——————      —————-

Car Mfr End       :                       ——————         ——————         ——————

(OEM)

Different Stages of Production at Co. End

a)                     :                       ——————              ——————              ——————

b)                     :                       ——————              ——————              ——————

c)                     :                       ——————              ——————              ——————

d)                     :                       ——————              ——————              ——————

e)                     :                       ——————              ——————              ——————

                                                                                                                              (Signature)

20 ) CHECK LIST FOR MATERIAL SPECIFICATION

 Part Name     :                                                                  Part Number :

 Customer      :                                                                  Vehicle / Model:

S.No.Check PointRequiredComments / Action RequiredResponsibilityDue Date
  YesNo   
1.Are Special Characteristics for materials been identified?     
2.Are specified materials, heat treat and surface treatments compatible with the product durability requirements? (For Design Companies only)     
3Are the intended materials suppliers on the customer approved list?     
4Will materials suppliers be required to provide Test Certificate / Report with each shipment?     
5.Have the materials characteristics requiring inspection been identified? If so:     
a)Will Characteristics be checked in-house?     
b)Is Test Equipment available?     
c)Will training be required to assure accurate result?     
6Will Out-side Laboratories be used for the purpose?     
7Are all Laboratories used accredited (if required)?     
8.Have the following materials requirements been considered?     
a)Handling     
b)Storage     
c)Environment during storage     
d)Identification during storage     

                                                                                                                        (SIGNATURE)

21) WORK INSTRUCTION FOR SPECIFIC PPAP REQUIREMENT

PURPOSE: To generate instruction for Customer Specific Requirements to perform PPAP Documents.

SCOPE: Applicable to all New Produced Parts, Correction of Discrepancy on previously submitted Parts & In case to change in part through Engineering change in design/specification/ material.                         

PPAP REQUIREMENTS:

Sr. No.PPAP DocumentsTo CustomersFrom Suppliers
Level-1Level-2Level- 3Level-4Level-5Non ISO/TSISO/TS
16949
1Product DrawingRSS*RSS
2Product SpecificationRSS*RSS
3Engineering change documents, if anyRSS*RSS
4Customer Engg. approval, if requiredRRS*R
5Process Flow ChartRRS*R
6Process flow diagramsRRS*RSS
7Process FMEARRS*RS
8Dimensional resultsRSS*RSS
9Customer Inspection Report (If Available)RSS*RSS
10Material performance Test resultsRSS*RSS
11Initial process studyRRS*RS
12Measurement system analysis studiesRRS*RS
13Qualified laboratory documentationRSS*S
14Control planRRS*RSS
15Part submission warrant (PSW)SSSSRS
16Appearance approval report,(AAR)
If applicable
SSS*
17Sample productRSS*RSS
18Master sample If availableRRR*R
19Packaging and Labelling  Std & Logistics       
20List of checking aids for all drawing dimnsRRR*R
21Records of compliance with customer- specific requirementsRRS*R
22Sub Supplier PPAP (s)       
         
  • If customer demands PPAP and does not specify level or requirements, Level 3 shall be considered as default level.
  • Level 4 shall be followed if customer does not specify the level but gives only specific requirements.
  • If customer does not demand PPAP, level 5 shall be followed.

*  If required by customer.

R: Retain      S: Submit

Perform only specific PPAP – if any of the following situations take place:

  • When an Optional construction or material than the previously submitted part in used.
  • When production is carried out using new or modified tooling (not the perishable tools).
  • When there is any rearrangement/ refurbishment of equipment / tooling.
  • When there is any change in process or method of manufacture that affects quality of end product.
  • When production is carried out from equipment /tooling transferred to different plant / location on from an additional plant / location.
  • When there is any change in source of subcontractor of non standard Part or material that affects end product quality.
  • When a production is carried out with a tooling inactive for last 12 month or more.
  • When there is any change in component or its process that affects end product quality.
  • When there is any change in Test / inspection methodology / technique