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Internal Quality Management Audit Report Report [insert #]

Environment Canada
Internal Quality Management Audit Report
Report No [insert number]

ISO 9001:2008
[Insert title and reference number of audited process]

[Insert date of audit]

Lead Auditor: ________________________

Process Owner: ________________________

(Insert name and number of process) (Insert date of audit)


PROTECTED A once filled Page 1 of 5
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Internal Quality Management Audit Report Report [insert #]

Overarching Process:
Underlying Process name:
Process Owner:
Auditee management
representative(s):
Lead Auditor:
Additional Audit Team
members:
Location/address of audit:

Scope of audit:
Start Date: End Date:

Audit Findings
No issues or non-conformances were identified during this assessment.
One or more non-conformances were identified.
One or more opportunities for improvement were identified.

Opening/Closing Meeting

Topics for Opening Meeting Topics for Closing Meeting

Review scope and objectives of audit Briefing on audit results


Review audit plan and methodology Review non conformances
Health and Safety Concerns Identify follow-up requirements
Time and Date for Closing Meeting

(Insert name and number of process) (Insert date of audit)


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Internal Quality Management Audit Report Report [insert #]

Audit Report

Opening Remarks

Report on setting of quality objectives and monitoring success:

Report on progress towards implementing continual improvement:

Report on customer feedback and responses (unsolicited or solicited):

Report on input to management review process and response to outcomes from that process:

Report on non-conformances identified in previous audit(s) and their current status:

(other reports at discretion of auditor)

(Insert name and number of process) (Insert date of audit)


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Internal Audit Assessment Report

Non-conformances

CPAR # Process/ISO
Summary description Internal QMS reference
see Note 1 Clause
• Requirements (process or ISO):
• Objective evidence:
• Process or ISO reference:

• Requirements (process or ISO):


• Objective evidence:
• Process or ISO reference:

• Requirements (process or ISO):


• Objective evidence:
• Process or ISO reference:

Note 1: CPAR number to be assigned by QMS Office after review of preliminary audit report.
Additional detail or clarifications on above non-conformances:
(may be filled out by auditors a the time of audit or by QMS staff upon review of preliminary report)

(Insert name and number of process) (Insert date of audit)


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Internal Audit Assessment Report

Opportunities for Improvement

Process/ISO
Summary description Internal QMS reference
Clause

Additional detail on above opportunities:

(Insert name and number of process) (Insert date of audit)


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