Hi all. We have been informed by the USFDA that they intend to audit a number of our sites here in the UK. We export product to the US so I am guessing that this is in connection with the Food Safety Modernisation Act. It appears to be members of the FDA that will be auditing so in preparation I have been trying to understand the standard that the FDA are expecting so we can gap assess against it. We currently have BRC accreditation but I am finding it very difficult to find a single document that defines the FDA requirements. Does anyone have any suggestions?
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