FDA Inspection 1100335 — Fareva Pau
The FDA completed an inspection of Fareva Pau on April 27, 2018 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
- April 27, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Idron (France)
Additional Details
Mutual Recognition Agreement (MRA)