FDA Inspection 1131392 — Biosint S.P.A.

Biosint S.P.A. — FEI 3002806601

The FDA completed an inspection of Biosint S.P.A. on Nov 23, 2018 in Sermoneta. 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 23, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sermoneta (Italy)

Additional Details

Mutual Recognition Agreement (MRA)