FDA Inspection 924404 — Trifarma S.P.A.

Trifarma S.P.A. — FEI 3002807260

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

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