Division 4.2
United Kingdom
The manufacturer shall, for assessment purposes, allow the F1approved body access to the manufacture, inspection, testing and storage sites and shall provide it with all necessary information, in particular:
- (a)
the quality system documentation;
- (b)
the quality records, such as inspection reports and test data, calibration data and qualification reports on the personnel concerned.
Annotations
Textual amendments
- F1
Word in Annex 8 para. 4.2 substituted (31.12.2020) by The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/696), reg. 1, Sch. 35 para. 3(51)(c); 2020 c. 1, Sch. 5 para. 1(1)
Notes on Division 4
Textual amendments
- F1
Word in Annex 8 para. 4 heading substituted (31.12.2020) by The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/696), reg. 1, Sch. 35 para. 3(51)(c); 2020 c. 1, Sch. 5 para. 1(1)