FDA Inspection 1268454 — Recipharm Pessac

Recipharm Pessac — FEI 3011269473

The FDA completed an inspection of Recipharm Pessac on Jun 28, 2024 in Pessac. 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
Jun 28, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pessac (France)

Additional Details

Mutual Recognition Agreement (MRA)