FDA Inspection 917710 — Suanfarma Italia S.p.A.

Suanfarma Italia S.p.A. — FEI 1000312133

The FDA completed an inspection of Suanfarma Italia S.p.A. on February 6, 2015 in Rovereto. 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 6, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rovereto (Italy)