GM1 21.A.126(b)(5) Production inspection system -- Engineering and manufacturing review procedure

Q: Under which point of Part 21 must the deviation be presented to the design approval holder?

Under the provisions of point 21.A.122.

Q: What must be recorded in the production inspection system procedure regarding the outcome of the design approval holder's review?

The results of the review and action taken consequently as regards the part/product must be recorded.

Q: In the context of GM1 21.A.126(b)(5), what is the required treatment for unintentional deviations from manufacturing or inspection data?

They should be recorded and handled in accordance with Part 21, Section A, Subpart D or E as changes to the approved design.

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GM1 21.A.126(b)(5) Production inspection system — Engineering and manufacturing review procedure

ED Decision 2022/021/R

(a) The procedure should permit to record the deviation, to present it to the design approval holder (DAH) under the provisions of point 21.A.122, and to record the results of the review and action taken consequently as regards the part/product.

(b) Any unintentional deviation from the manufacturing/inspection data should be recorded and handled in accordance with Part 21, Section A, Subpart D or E as changes to the approved design.

Details

Source-Title: GM1 21.A.126(b)(5) Production inspection system -- Engineering and manufacturing review procedure View latest amendments

Erulesid: ERULES-1963177438-3795 Compare versions

Domain: Initial airworthiness

Amendedby: Issue 2, Amendment 14

Applicabilitydate: 7 March, 2023

Entryintoforcedate: 20 December, 2022

Regulatorysource: ED Decision 2022/021/R Navigate

Regulatorysubject: Part-21

Typeofcontent: GM to IR (Guidance material to implementing rule)

Origin: EASA

Category: EAR