Example of documentation template for process of Internal audit

The following document templates (tool kits) are provided totally complimentary, free of charge to use as a starting point for Process of Internal Audit 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 Internal Audit

2.0 Turtle Diagram of Process of Internal Audit

3.0 Non- Compliance Report

DATE:-                                                                         
 SL. NO.——–
  DEPTT./FUNCTION          :-  
AUDITEE                           :-  
AUDITOR (S)                     :-  
NON- COMPLIANCE AGAINST CLAUSE NO:-  
NON- COMPLIANCE DETAILS:  


SIGN: (AUDITEE)                                                                                                            

SIGN (AUDITOR)  


CORRECTION (IMMEDIATE ACTION)-IF POSSIBLE



ROOT CAUSE :


PLANNED CORRECTIVE & PREVENTIVE ACTION


TARGET DATE:-                                                                                                            


SIGN. (AUDITEE)  




CORRECTIVE ACTION IMPLEMENTED AND EFFECTIVE  DATE


                                                                                                                                           
SIGN. (AUDITOR)                                     
NON- COMPLIANCE REPORT CLOSED                                                                                                           


SIGN M.S

4.0 INTERNAL AUDIT SCHEDULE                    

Date:

Subject: IATF 16949/2016 Internal Audit

SR.NOAUDITORAUDITEEAUDIT
CRITERIA
DEPT.TIME SHIFT A/BDATE
       
       
      
      
      
      
 
      
      
      
      
 
      
      
      
                

The persons whose names are written above mention are requested to be follow Audit Plan  

 Name   

Sign

REGARDS

Cc: Directors (For your kind information pl)

5.0 Internal Quality Audit Plan

        INTERNAL QUALITY AUDIT PLAN FOR THE YEAR……
      Sr. No.    Department/ Function  MONTHS      Remarks
  Apr.10  Mai.10  Jun.10  Jul.10  Aug.10  Sep.10  Okt.10  Nov.10  Dez.10  Jän.11  Feb.11  Mär.11
               
               
               
               
               
               
               
               
               
               
               
               
               
               
  Prepared by      Approved by

6.0 Product Audit Plan Cum Schedule

Company Name   Date:
S.No.Part NameDateTimeAuditeeAuditorAprMayJunJulAugSepOctNovDecJanFebMar
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
                  
  Prepared By:         Approved By :

7.0 System Audit Report

SYSTEM AUDIT REPORT/NOTES
AUDIT NO. : 
FUNCTION/ AREA / PROCESS: 
AUDITOR(S) :
AUDITEE(S) :
  S.NOAUDIT FINDINGS : Record technologies/ process, inputs /outputs / internal external customers, CSR, Issues, risk, system deficiencies, positive & negative observation & any follow up audit activities required.CLAUSE NO. (in case of NC)  STATUS
  












































  
NC = NonconformityC = Conformity
OI = Opportunities for Improvement 
DateAuditorAuditee
   

8.0 Manufacturing Process Audit Report

DepartmentMachine Name                                                           Date of Audit
Process NameProduct Name                                                             Part No
Sr NoCHECK POINTSPEC/ TARGETACTUALAUDITOR OBSERVATIONREMARKS
APROCESS PARAMETER
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
PROCESS CONTROL
BCHECK POINTAUDITOR OBSERVATIONREMARKS
  1  Are documented W.I/CP displayed and used all the correct location covering quality &saftey points ?  
2  Knowledge of WI instruction /OS to operater  
3Is product lot identified and traceable w.r.t.material?  
4Knowledge to operater about instrument/ gauge /calibration  
5Checked the work instruction & OS are avaliable on machine  
6  Records / petrolling report/ setting report  
7Are device calibrated with status?  
AUDITOR SIGN.                                                                                                            AUDITEE SIGN.

9.0 Product Audit Report

Part NameDate
Drawing NoAuditor
Dept .NameAuditee
Product Characteristics
Sr NoDimSpecficationInspector ObservationAuditor observationstatus
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
Gauge /Instrument Calibration Status
Sr NoDescriptionID CodeCalibration ObservationStatus
     
     
Records / Reports Verification
Sr NoRecordsObservationstatus 
1Patroling Records   
2Operation standard   
3Setting Approval   
Packing & Labelling
Sr NoDescripationObservationstatus 
     
     
Auditor  Auditee

10.0 Internal Audit Summary Report

  IATF 16949 INTERNAL AUDIT SUMMARY REPORT         MONTH :
SL. No.DATE OF AUDIT  DEPT.OBSERVATION / NON CONFORMITY DETAIL  REASON  ACTION PLAN  RESPONSIBILITY  T DSTATUS AS ON DATE
        
         
         
         
         
         
         

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