FDA Inspection 1253273 — Pierre Fabre Pharmaceuticals, Inc.

Pierre Fabre Pharmaceuticals, Inc. — FEI 3013144400

The FDA completed an inspection of Pierre Fabre Pharmaceuticals, Inc. on Nov 1, 2024 in Parsippany, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 1, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Parsippany, NJ (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

Citations

IDCFRDescription
1802821 CFR 314.80(f)(4)Incomplete initial reporter information on ICSR
673221 CFR 314.80(c)(1)(i)Late submission of 15-day report