F-MR-11 Non Conformity Report
F-MR-11 Non Conformity Report
F-MR-11 Non Conformity Report
F/MR/11
Eff. Date
00
01/01/17
Non -
Conformity-
Type of Audit: QMS Audit Product Audit Process Audit External Audit (Specify)- Supplier Audit
Status
Date Corrective Action Verification/Follow up Comment
Open/Closed Sign. Auditor
Non -
Conformity-
Ref. Procedure /
Objective Doc.
Evidence-
Type of Audit: QMS Audit Product Audit Process Audit External Audit (Specify)-
Effected Documents –
1. PFMEA 2. Control Plan 3. Process Cont. Standard 4. Work Instruction 5. Q Manual/Procedure 6. Format 7. Other
Status
Date Corrective Action Verification/Follow up Comment
Open/Closed Sign. Auditor
Non -
Conformity-
Ref. Procedure /
Objective Doc.
Evidence-
Type of Audit: QMS Audit Product Audit Process Audit External Audit (Specify)-
Effected Documents –
1. PFMEA 2. Control Plan 3. Process Cont. Standard 4. Work Instruction 5. Q Manual/Procedure 6. Format 7. Other
Status
Date Corrective Action Verification/Follow up Comment
Open/Closed Sign. Auditor
Format No. F/MR/11
Non -
Conformity-
Ref. Procedure /
Objective Doc.
Evidence-
Type of Audit: QMS Audit Product Audit Process Audit External Audit (Specify)-
Effected Documents –
1. PFMEA 2. Control Plan 3. Process Cont. Standard 4. Work Instruction 5. Q Manual/Procedure 6. Format 7. Other
Status
Date Corrective Action Verification/Follow up Comment
Open/Closed Sign. Auditor
Non -
Conformity-
Ref. Procedure /
Objective Doc.
Evidence-
Type of Audit: QMS Audit Product Audit Process Audit External Audit (Specify)-
Effected Documents –
1. PFMEA 2. Control Plan 3. Process Cont. Standard 4. Work Instruction 5. Q Manual/Procedure 6. Format 7. Other
Status
Date Corrective Action Verification/Follow up Comment
Open/Closed Sign. Auditor
Non -
Conformity-
Ref. Procedure /
Objective Doc.
Evidence-
Type of Audit: QMS Audit Product Audit Process Audit External Audit (Specify)-
Effected Documents –
1. PFMEA 2. Control Plan 3. Process Cont. Standard 4. Work Instruction 5. Q Manual/Procedure 6. Format 7. Other
Status
Date Corrective Action Verification/Follow up Comment
Open/Closed Sign. Auditor
Non -
Conformity-
Ref. Procedure /
Objective Doc.
Evidence-
Type of Audit: QMS Audit Product Audit Process Audit External Audit (Specify)-
Effected Documents –
1. PFMEA 2. Control Plan 3. Process Cont. Standard 4. Work Instruction 5. Q Manual/Procedure 6. Format 7. Other
Status
Date Corrective Action Verification/Follow up Comment
Open/Closed Sign. Auditor
Non -
Conformity-
Ref. Procedure /
Objective Doc.
Evidence-
Type of Audit: QMS Audit Product Audit Process Audit External Audit (Specify)-
Effected Documents –
1. PFMEA 2. Control Plan 3. Process Cont. Standard 4. Work Instruction 5. Q Manual/Procedure 6. Format 7. Other
Status
Date Corrective Action Verification/Follow up Comment
Open/Closed Sign. Auditor
Format No. F/MR/11
AQE AUDIT NON–CONFORMITY REPORT Rev. No.
Eff. Date
00
01/01/17
Non -
Conformity-
Ref. Procedure /
Objective Doc.
Evidence-
Type of Audit: QMS Audit Product Audit Process Audit External Audit (Specify)-
Effected Documents –
1. PFMEA 2. Control Plan 3. Process Cont. Standard 4. Work Instruction 5. Q Manual/Procedure 6. Format 7. Other
Status
Date Corrective Action Verification/Follow up Comment
Open/Closed Sign. Auditor
Non -
Conformity-
Ref. Procedure /
Objective Doc.
Evidence-
Type of Audit: QMS Audit Product Audit Process Audit External Audit (Specify)-
Effected Documents –
1. PFMEA 2. Control Plan 3. Process Cont. Standard 4. Work Instruction 5. Q Manual/Procedure 6. Format 7. Other
Status
Date Corrective Action Verification/Follow up Comment
Open/Closed Sign. Auditor