FDA Inspection 856416 — Trifarma S.p.A.

Trifarma S.p.A. — FEI 1000532829

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