FDA Inspection 1287752 — Finorga

Finorga — FEI 3002806998

The FDA completed an inspection of Finorga on November 24, 2023 in Mourenx. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 24, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mourenx (France)

Additional Details

Mutual Recognition Agreement (MRA)