FDA Inspection 924404 — Trifarma S.p.A.

Trifarma S.p.A. — FEI 3002807260

The FDA completed an inspection of Trifarma S.p.A. on February 27, 2015 in Rozzano. 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
February 27, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rozzano (Italy)