Pierre Fabre Medicament — FDA Facility Profile

FEI 3002807889

Pierre Fabre Medicament is an FDA-registered facility (FEI 3002807889) located in Occitanie, FR. Registered operations: API MANUFACTURE. RegDataLab tracks 4 FDA inspections at this facility.

Facility Details

Location
Occitanie (FR)
Registration Expires
Dec 31, 2026
Operations
API MANUFACTURE
Source
decrs