Paragraph 4.2 F1
The manufacturer shall for assessment purposes allow the approved body access to the premises where final inspection, testing and storage are carried out and provide it with all necessary information, in particular:
(a)
the quality system documentation;
(b)
the technical documentation;
(c)
the quality records, such as inspection reports and test data, calibration data, reports on the qualifications of the personnel concerned.
Annotations
Textual amendments
- F1
Schs. 11-19 inserted (E.W.S.) (31.12.2020) by The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/696), reg. 1, Sch. 22 para. 44 (with Sch. 22 para. 37) (as amended by S.I. 2020/676, regs. 1(1), 2); 2020 c. 1, Sch. 5 para. 1(1)