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Audit Notification
Audit Number:- Title:- Location:- Date:-
Review of Quality Management Plan, Manufacturing Procedures, and Inspection and Test Plan
Review of requirements as per specifications and project specific procedures. Verify availability of project
specifications and project specific procedures.
Verification of status of submission/approval of deliverable documents in accordance with the SDR
Control of Documents / Records
Quality control and production personnel competency review.
Quality control processes including identification and traceability, in-process, final inspections and
inspection release process;
Control of calibration of equipment and measuring devices
Control of Non-Conforming Products. Verification of NCR process (Internal, External, Customer issued) log
and close-out
Internal and external audit process; Verification of audits and audit plan
Change management / TQ management and control process
Management and control of sub-suppliers
Equipment/Material Storage, Handling & Preservation
Verification of Manufacturers Record Book, progressive compilation, MRB Index
HSE
Tour of facility
Reference Documents (Basis of Audit)
1. Unpriced PO
2. Purchase Requisition
3. ITP
4. SDR
5. Quality Manual
Audit Team Leader:- Audit Program (Date and Time)
MDR-GLOBAL-FORMS-QHSES-038
Comments.
An audit is scheduled on the subject(s) listed above at the date(s) and time(s) shown. Those persons indicated as
Auditees are requested to confirm their availability to attend the audit and entry meeting by signing their names
below. The detailed timetable showing the required involvement of individuals in the audit will be presented and
agreed at that meeting.
Arrangements Confirmed for Audit Team:- Arrangements Confirmed for Audit Auditee:-
MDR-GLOBAL-FORMS-QHSES-038