Example of documentation template for process of Control Of Non Conforming Products

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Process of Control Of Non Conforming Products 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 Control of Non Conforming Products

2.0 Turtle diagram of Control of Non Conforming Products

3.0 Corrective & Preventive Action ( 8-Discipline Report)

Part Name Model 
Part No. Supplier part No. 
Drg. Ref. Drg. Modification status 
Date Feedback form 
(1) PROBLEM AWARENESS
Problem ScopeProblem SeverityProblem Source                                           % Defect
  New Safety   
Regulatory 
Functioonal   
  Existing Aesthetic 
Reliability   
  Reopened 
Others   
(2) PROBLEM DEFINITION
 
(3) CONTAINMENT ACTION / SHORT TERM ACTION
NO.Immediate Action TakenCompletionResponsibleDate
     
     
(4) ROOT CAUSES (ttached root cause analysis Sheet -Fish Bone, Brainstorming,Pareto analysis,Why-Why analysis etc.)
 
(5) CORRECTIVE ACTIONS VERIFICATIONDATEMETHODRESULTS
  TARGETEFFECTIVE  
     
     
     
     
     
     
(6) PREVENTION (6) VERIFICATIONDATEMETHODRESULTS
 RESPONSIBILITYTARGETEFFECTIVE  
     
     
     
     
     
(7) REVIEW -DOCUMENTS / SYSTEM(Attach copies of all revised documents)
No.QMS DOCUMENTIF YESRESPONSIBLEPLANNED DATEACTUAL DATESTATUS
1Control Plan     
2Process sheet     
3Drawing / Process flow diagram     
4PFMEA / DFMEA / PPAP     
5Process Map     
6Acceptance Standard     
7PM checklist     
8Work Instruction / Calibration Plan     
(8) PROBLEM CLOSURE & SIGN-OFF
PROBLEM PROGRESS SUMMARYCLOSURE SIGN-OFF
S.No.PhaseStart dateEnd dateTeam MemberAreaSign-off
1Problem Definition     
2Containment action     
3Root cause analysis     
4Corrective action     
5Solution confirmation     
6Closure     
MANAGEMENT VERIFICATION & CLOSURE
Sign     
Date     
Name     
HeadManufacturing ChiefQuality ChiefDesign chiefmanagement RepresntativePlant Head

4.0 Deviation Request

DEPT.                                                                               
PROCESS/AREA :                                                   
DATE:                                 
TIME:    
MACHINE :                                                             
PART DESCRIPTION :                                             

PART NO:    
CUSTOMER:                                                                                         

IR NO:                                                     
DEV. QTY:  
LOT NO :                                                                                         
MRN NO:                       

MATERIAL:                          

GRADE/FINISH :
NATURE OF DEVIATION    REASON
  S.NO.  PARAMETER  SPECIFICATION  ACTUAL
     









  REQUESTED BY:
  DETAILS OF ATLEAST 3 PREVIOUS LOTS
  S.No  Supplied Qty  Actepted Qty.  Rej Qty.  Deviation if Any
     






CORRECTIVE ACTION SUGGESTED
ACTION PLANRESP.TG. DATESIGN
    
    
    
    
    
    
    
    
    
CORRECTION & DISPOSITION:  
ACCEPTED UNDER DEVIATION WITH /WITHOUT REPAIR:  
TO BE REWORKED /CHANGED:  
REGRADED FOR ALTERNATIVE APPLICATION:  
REJECTED OR SCRAPPED:  
TO BE SORTED NOW/ LATER STAGE:
FINAL REMARKS        
 DISPOSITION AUTHORITY

5.0   Disposal Note cum Rework Data

DISPOSITION AUTHORITY:
Deptt.:-     Period :-
S.No.Part NameProdRej Pcs.PPM (Rej.)Nature of Rej.Root causeAction PlanCost/pieceTotal Rej.costRework Pcs.PPM (Rew.)Nature of Rework.Root causeAction PlanRemarks
         0      
         0      
         0      
         0      
         0      
         0      
         0      
         0      
         0      
         0      
         0      
         0      
         0      
         0      
         0      
Prepared ByVerify ByApproved by (DGM)Approved by ( Director )