FDA Inspection 822697 — Pierre Fabre Medicament

Pierre Fabre Medicament — FEI 3002807889

The FDA completed an inspection of Pierre Fabre Medicament on Mar 14, 2013 in Gaillac. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 14, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gaillac (France)