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[F1SCHEDULE 7E+W+S(Annex II to the Directive)

CONFORMITY ASSESSMENT PROCEDURESE+W+S

3.6.2.  The manufacturer shall, for assessment purposes, allow the approved body access to the manufacture, inspection, testing and storage sites and shall provide it with all necessary information, in particular—E+W+S

(a)the quality system documentation;

(b)the technical documentation referred to in point 3.2;

(c)the quality records, such as inspection reports and test data, calibration data, qualification reports on the personnel concerned, etc.]