ISO 9001 Documents
ISO 9001 Documents
ISO 9001 Documents
Document ID: Appendix A / Page: 1 of 5/Rev. No.: 00/ Rev. Date: 01-03-2008
Appendix A
Clause No. Document No. R-5.6 DFC 6.2 R-6.2 A 6.2 R-6.2 B R-6.2 C R-6.2 D DFC 6.3 R-6.3 7.1 7.2 7.3 DFC 7.1 DFC 7.2 SOP 7.3
Second Level Documents Document Title Yearly Plan for Management Review and internal Quality Audit Human Resource Development Competence requirement for Human resources Skill Matrix Questionnaire for Leadership Evaluation Questionnaire for Internal Auditor Evaluation Methodology for Resource Maintenance List of Machinery with their capability Product Realization Processes Review of product related requirements (contract review) Methodology for Product Design and Development Mkt-01 M-13 MT-01 M-11 M-12 R-6.2 B Form No.
Forms for Records Form Title Review Employee Card Training Attendance Sheet Skill Matrix
6.3, 6.4
Document ID: Appendix A / Page: 2 of 5/Rev. No.: 00/ Rev. Date: 01-03-2008
Appendix A
Forms for Records Form Title Evaluation and Selection of Supplier List of Supplier with Grade Periodic Re-evaluation of Supplier Purchase Order
7.4.1
SOP 7.4.1
Methodology for Evaluation and Reevaluation Purchasing Production Flow Chart Control of Production Processes
PR-02 PR-03
SOP 7.4.2 DFC 7.5.1 SOP 7.5.1 Exclusion SOP 7.5.3 SOP 7.5.4 SOP 7.5.5 SOP 7.6 R-7.6
PO
Methodology for Product identification and Traceability Control of Customer Property Methodology for Preservation of Product Methodology for control of monitoring and measurement devices List of Monitoring and Measurement Devices
-------
Document ID: Appendix A / Page: 3 of 5/Rev. No.: 00/ Rev. Date: 01-03-2008
Appendix A
Clause No. Document No. 8.2.1 SOP 8.2.1 P-IQA 8.2.2 R-5.6 ---R-5.4.1 8.2.4 PQP-1 PQP-2 PQP-3 8.3 8.4 8.5.2, 8.5.3 P-NCP DFC 8.4 P-CPA
Second Level Documents Document Title Methodology Customer Satisfaction Survey Procedure for Internal Quality Audit Yearly Plan for Management Review and internal Quality Audit All DFCs and SOPs Quality Objectives Product Quality Plan Receiving Stage Product Quality Plan In-process Stage Product Quality Plan Final Stage Procedure for Control of Non conforming products Analysis of Data Procedure for Corrective and M-08 M-08 Form No.
Customer Feedback Form Internal Audit Schedule Internal Audit Report Action Request (AR) Monitoring of Processes of QMS Quality Objectives
8.2.3
Document ID: Appendix A / Page: 4 of 5/Rev. No.: 00/ Rev. Date: 01-03-2008
Appendix A
Forms for Records Form Title Supplier Corrective Action Request (SCAR) Corrective - Preventive Action (CPA)
M-09 M-10
Document ID: Appendix A / Page: 5 of 5/Rev. No.: 00/ Rev. Date: 01-03-2008