FDA Inspection 1257030 — Orgapharm

Orgapharm — FEI 3002807503

The FDA completed an inspection of Orgapharm on Mar 17, 2022 in Pithiviers. 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 17, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pithiviers (France)

Additional Details

Mutual Recognition Agreement (MRA)