FDA Inspection 1288688 — Trifarma S.p.A.

Trifarma S.p.A. — FEI 1000532829

The FDA completed an inspection of Trifarma S.p.A. on April 7, 2023 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
April 7, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ceriano Laghetto (Italy)

Additional Details

Mutual Recognition Agreement (MRA)