FDA Inspection 856416 — Trifarma S.P.A.

Trifarma S.P.A. — FEI 1000532829

The FDA completed an inspection of Trifarma S.P.A. on Nov 15, 2013 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
Nov 15, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ceriano Laghetto (Italy)

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