FDA Inspection 1060492 — Orgapharm

Orgapharm — FEI 3002807503

The FDA completed an inspection of Orgapharm on Jun 7, 2018 in Pithiviers. 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
Jun 7, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pithiviers (France)