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Home » The Right Response to an FDA Inspectional Report May Avert a Warning Letter
The Right Response to an FDA Inspectional Report May Avert a Warning Letter
A device manufacturer that undergoes an FDA inspection and gets a Form 483 with findings may avert a warning letter from the agency if it “really responds well,” said Jodi Scott, a partner at Hogan Lovells US, speaking Wednesday at the WCG and FDAnews-sponsored FDA Inspections vSummit.