FDA Inspection 1135715 — Trifarma S.p.A.
The FDA completed an inspection of Trifarma S.p.A. on January 31, 2020 in Ceriano Laghetto. 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
- January 31, 2020
- Fiscal Year
- 2020
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Ceriano Laghetto (Italy)
Additional Details
Mutual Recognition Agreement (MRA)