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This Audit Report Template has been created according to the ISO 19011:2018, ISO 13485 and 21 CFR Part 820.
It contains predefined sections and provides recommended guidance for filling in content.
It can be used by both medical device organizations and any other organization that conducts internal and / or supplier audits.
12 pages
It contains predefined sections and provides recommended guidance for filling in content.
It can be used by both medical device organizations and any other organization that conducts internal and / or supplier audits.
12 pages