21 C.F.R. § 1.680

How and when will FDA monitor eligible entities?

Last amended: 2016Year: 2026Length: 83 wordsOfficial source

Cite as 21 C.F.R. § 1.680 (2026)

FDA may, at any time, conduct an onsite audit of an eligible entity that has received food or facility certification from an accredited third-party certification body under this subpart. Where FDA determines necessary or appropriate, the unannounced audit may be conducted with or without the accredited third-party certification body or the recognized accreditation body (where applicable) present. An FDA audit conducted under this section will be conducted on an unannounced basis and may be preceded by a request for a 30-day operating schedule.
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