FDA Inspection 1135715 — Trifarma S.P.A.

Trifarma S.P.A. — FEI 1000532829

The FDA completed an inspection of Trifarma S.P.A. on Jan 31, 2020 in Ceriano Laghetto. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 31, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ceriano Laghetto (Italy)

Additional details

Mutual Recognition Agreement (MRA)

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