What Not To Do When An FDA Inspector Knocks At Your Door

FDA tweaks its guidance on what constitutes interference with inspections to include examples of “reasonable” explanations for delays. But industry requested other changes, including a formal process for notifying a firm of FDA’s intent to deem products adulterated due to delaying, limiting or refusing an inspection.

FDA’s final guidance on describing interference with FDA inspections that may cause a drug to be deemed adulterated includes examples of “reasonable” explanations for sponsor behavior that causes delays, but largely ignores industry concerns that the document is overreaching.

The guidance announced in an Oct. 22 Federal Register notice, “Circumstances that Constitute Delaying, Denying, Limiting, or Refusing...

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