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Check List For QMS Internal Audit

This audit checklist summarizes the activities and documentation required to maintain an ISO 9001 quality management system. It addresses sections including housekeeping, quality planning, management responsibility, resource management, product realization, measurement and improvement. For each section, it lists key requirements and asks auditors to verify whether documentation and activities adhere to the standard. The checklist is signed by the auditor and management representative to confirm the audit was completed.

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100% found this document useful (3 votes)
1K views4 pages

Check List For QMS Internal Audit

This audit checklist summarizes the activities and documentation required to maintain an ISO 9001 quality management system. It addresses sections including housekeeping, quality planning, management responsibility, resource management, product realization, measurement and improvement. For each section, it lists key requirements and asks auditors to verify whether documentation and activities adhere to the standard. The checklist is signed by the auditor and management representative to confirm the audit was completed.

Uploaded by

Tanzila Siddiqui
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as DOC, PDF, TXT or read online on Scribd
You are on page 1/ 4

Date: 15/02/2019 ISO - 9001 ALM – QMS DOC # 09-E

Audit Checklist
Date: _______________________

Section
Contact Person
Manpower: Officers: Staff /Worker:
AUDIT CHECK LIST
A. HOUSE KEEPING
No. Activity Yes No Remarks
a. General Cleaning and House Keeping
B. QUALITY MANAGEMENT SYSTEM (SECTION 4)
No. Activity Yes No Remarks
a. Is quality plan / process flow chart available?
c. Is procedure for control of document available?
d. Are work instructions available?
e. Is procedure for control of record available?
C MANAGEMENT RESPONSIBILITY (SECTION 5)
No. Activity
i. Is quality policy available?
ii. Are employees know about quality policy?
iii. Are job description available?
iv. Is quality management representative appointed?
v. Is organization chart available?
vi. Is management review board formed?
vii. Is record of management review meetings available?
ix. Is internal communication Memo Verbal Phone
system available?
x. Is quality system manual available?
xi. Are quality system procedures available? .
xii. Are documents controlled?
xiii. Is system of verification of approval of document and data
exist?
xiv System of distribution of document & data available.
xvi Is system to incorporate changes in documents exist?
xvii Is system to control & identify obsolete documents exist.
xviii Is list of file / records maintained?
xix Is the record retention period of record set up?
C. RESOURCE MANAGEMENT (SECTION 6)
No. Activity Yes No Remarks
i. Is training plan available?
Ii Is training attendance maintained?
iii Is training material available?
vii. Is maintenance of workplace, associated facilities and
support services carried out.
viii Is conducive work environment maintained?
ix. Are first aid boxes available?
xi. Are records of supporting services like transport and

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Date: 15/02/2019 ISO - 9001 ALM – QMS DOC # 09-E

communication maintained.
D. PRODUCT REALIZATION (SECTION 7)
7.1 PLANNING OF PRODUCT REALIZATION
No. Activity Yes No Remarks
i. Quality Objectives Department wise Section
wise
ii. Are Contract records maintained?
7.2.1 DETERMINATION OF REQUIREMENT RELATED TO THE PRODUCT
i. Is purchase order received form customer?
ii. Is the purchase assessed?
iv. Is customers defined regulatory requirements entertained?
7.2.2 REVIEW OF REQUIREMENT RELATED TO THE PRODUCT
i. Is purchase order reviewed before acceptance?
ii. Is records of review exists?
iii. Is amendment (if any) communicated to customer?
7.2.3. CUSTOMER COMMUNICATION
i. Is the customer is immediately communicated about purchase
order compliance or etc.?
iii. Is customer feedback system existing?
iv. Is customer complaints handling procedures exists?
7.3 DESIGN DEVELOPMENT ………. Not applicable
I Are records of all activities of design development
maintained?
7.4 PURCHASING
i. Is the record of indents available?
ii. Is list of items available?
iii. Is clear specifications defined on indent?
iv. Is record of purchases made through cash available?
v. Is the procedure for purchases available?
vi. Is record of purchase orders / forecast available?
7.5.1 CONTROL OF PRODUCTION AND SERVICE PROVISION
i. Is availability of information about work to be performed
available?
iii. Are suitable equipment available?
iv. Are list of measuring devices (balances) available?
7.5.2 Validation of processes for production & service provision … Not applicable
7.5.3 IDENTIFICATION AND TRACEABILITY
i. Is system for product / service identification exist?
ii. Is identification of purchased materials carried out?
iii. Is identification of final product carried out?
vi. Is traceability of service / product carried out?
v. Is records of traceability of product maintained?
7.5.4 CUSTOMER PROPERTY ………. not applicable
i Are records of customer property maintained?
7.5.5 PRESERVATION OF PRODUCT
i. Are the appropriate step taken for storage of product?
Ii Is the products handling carried throughout the process
satisfactorily?
iii. Is the storage area identified?
v. Are the letter / reports / material dispatches are carried out

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Date: 15/02/2019 ISO - 9001 ALM – QMS DOC # 09-E

satisfactorily?
vi. Are the records of product delivery maintained?
7.6 CONTROL OF MONITORING AND MEASURING DEVICES
i. Is there a control on test equipment’s exist?
ii. Is there a master list of inspection and test equipment’s?
iii Are the instruments / equipment’s / machines in calibrated
conditions?
iv. Is the calibration record maintained?
v. Are calibrated instruments properly identified through
Stickers?
8. MEASUREMENT, ANALYSIS AND IMPROVEMENT (SECTION 8)
8.1 GENERAL
i. Is the production / service processes demonstrate conformity
with customer requirement?
8.2.1 CUSTOMER SATISFACTION
i. Is the customer satisfaction analyzed?
ii. Is there any evidence on appropriate actions on customer
feed backs / complaints?
iii. Is the customer on tri-month basis are provided with
feedback form for assessing the perception of organization?
8.22 INTERNAL AUDIT
i. Is the internal audit procedures available?
iii. Is the audit plan available?
iv. Are audit performed by personnel independent of the activity
being audited?
vi. Are audit reports properly documented?
8.2.3 MEASUREMENT AND MONITORING OF PROCESS
i. Is the inspection plan exist?
ii. Is the specification / diagrams for process monitoring and
measurement available?
iv. Is in-process inspection carried out?
V Is final inspection / checking carried out?
vi. Is the record of inspection and checking maintained?
vii. Is the record of corrective action taken to ensure the
conformity of results are available?
8.2.3 MEASUREMENT AND MONITORING OF PRODUCTS
i. Is the accuracy of the product verified?
ii. Is the record of final inspection and inspection criteria
maintained /
iii. Is the service / production data are authenticated for issue
before release?
8.3 CONTROL OF NON-CONFORMING PRODUCTS
i. Is the non-conforming product identified & recorded?
ii. Is re-checking of non-conforming product made?
iii. Is the nonconforming product /data results segregated?
8.4 ANALYSIS OF DATA
i. Is the customer satisfaction analyzed?
ii. Is statistical techniques used for data analysis.
iv. Are customers feed backs analyzed, recorded and
maintained?

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Date: 15/02/2019 ISO - 9001 ALM – QMS DOC # 09-E

8.5 IMPROVEMENT
8.5.1 CONTINUAL IMPROVEMENT
i. Is the quality policy and quality objectives are used for
continuous improvement?
ii. Is the audit finding are used for purpose of continuous
improvement?
8.5.2 CORRECTIVE ACTION
i. Is documented procedure available?
ii. Is corrective action taken on internal nonconformity?
iii. Is corrective action taken on customer complaints?
iv. Is causes of non-conformities determined?
v. Is record of corrective action is available?
vi. Is evaluation of corrective action is made?
8.5.3 PREVENTIVE ACTION
i. Is documented procedure available?
ii. Is preventive action is properly followed up?
iii. Is the record of preventive action maintained?
iv. Are corrective and preventive actions discussed in
management review meeting?

SIGNATURE OF AUDITOR: _______________________________

SIGNATURE OF MR: _______________________________

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