FDA Inspection 1202791 — Fareva Pau

Fareva Pau — FEI 3002806390

The FDA completed an inspection of Fareva Pau on November 5, 2021 in Idron. 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 5, 2021
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Idron (France)

Additional Details

Mutual Recognition Agreement (MRA)