QMS Inspection Procedure
QMS Inspection Procedure
QMS Inspection Procedure
uk
Quality Procedure
Testing & Inspection
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Table of Contents
1 TESTING & INSPECTION ........................................................................................................................... 3
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1.1.2 References
Standard Title Description
BS EN ISO 9000:2015 Quality management systems Fundamentals and vocabulary
BS EN ISO 9001:2015 Quality management systems Requirements
BS EN ISO 9004:2018 Quality management systems Guidelines for performance improvements
Verification Confirmation, through the objective evidence (3.8.3), requirements (3.6.4) were fulfilled
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1.3 Responsibilities
The Quality Manager is required to:
1. Determine the extent and scope of in-process inspection and testing;
2. Determine the extent and scope of product inspection and testing;
3. Ensure that planned arrangements are satisfactorily completed prior to release.
4. Ensure that this procedure is implemented.
The Quality Inspectors are required to:
1. Undertake inspection and testing in accordance with specified requirements;
2. Preserve the identification of inspected and testing products.
The received containers are then moved to the designated inspection area, a copy of the purchase order is
retrieved, and the packing slips are removed from the containers. Upon opening the containers, the goods are
verified against the purchase order and the packing slip, and are examined visually for any signs of damage.
The purchase order is stamped ‘RECEIVED’ and is signed and dated by the receiving inspector. All receiving
inspections are recorded using the Receiving Inspection Log. On critical parts and components, as determined
by the Quality Manager, a precision inspection and tests are performed. This type of inspection includes:
1. Review of relevance material certificates, supplier inspection records and compliance certificates;
2. Random sampling based on statistical technique specified;
3. Visual inspection to detect any damage or other visible problems;
4. Perform measurements and testing against specified requirements as required;
5. Record sample size, measurement and inspection test results using the Inspection & Test Report.
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Any products or services supplied wrongly supplied, damaged or not in accordance with the purchase order
requirements are documented onto a Defective Part Report and processed accordingly.
All purchased material which influences the manufacture of, or is intended for use as part of, deliverable
products is subject to inspection and testing by Quality Inspection Personnel.
1. Examine all critical dimensions affecting product performance for length, distance, outside diameter,
inside diameter, threads, taper, angle, height, depth, width, surface finish, diameter and radii;
2. Fit and function test the machining processes using the test or sample parts when specified on the
drawings;
3. Perform a first article inspection on each consecutive part until a part has been produced which is
within the target range for all dimensions;
4. Initial or stamp the dimensional record and/or traveller sheet with acceptance of the process when a
successful first article inspection is achieved for the particular work in progress.
All first article inspections are recorded in the First Article Inspection Log and are retained to provide traceability,
while any non-conformances are documented using the Defective Part Report and processed accordingly.
All products are inspected and tested as required by the work order and/or documented procedures. The scope
of the in-process inspection is determined by the Quality Manager, and is communicated to each work area
on the work order. As a minimum, the scope comprises:
1. Hold products until the required inspection has been completed and verified;
2. Review of the work order to ascertain that all specified operations, processes and first part
inspections are signed-off;
3. Verify that applicable documents are available and traceable to the product;
4. Visual inspection of product to ascertain that all specified operations are complete and to detect any
visible quality problems.
The Quality Manager determines the extent and scope of in-process inspection and testing based on the
importance of the item, control methods and previous performance. All in-process inspections are recorded
using the In-process Inspection Log. Any non-conformances are documented using the Defective Part Report
and processed accordingly.
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