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FDA Inspection
•Pierre Fabre Pharmaceuticals, Inc.•December 30, 2015

Pierre Fabre Pharmaceuticals, Inc. – FDA Inspection, Dec 30, 2015

Record Details

This FDA Inspection record concerns Pierre Fabre Pharmaceuticals, Inc., with an inspection on December 30, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Pierre Fabre Pharmaceuticals, Inc.
Inspection Date
December 30, 2015
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 140fdda4-ba34-4f68-82d6-163a0645a609

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
956345
FDA center
Human Drugs
Project area
Bioresearch Monitoring

FDA Citations

1
  1. 21 CFR 314.80(c)(1)(i)Late submission of 15-day report

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Pierre Fabre Pharmaceuticals, Inc.

2
DateClassificationOfficeProject area
November 1, 2024VAINew Jersey District OfficePostmarketing Surveillance and Epidemiology: Human Drugs
July 27, 2022VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Pierre Fabre Pharmaceuticals, Inc.
  • FDA Inspection 1253273 - 2024-11-01
  • FDA Inspection 1175515 - 2022-07-27

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