FDA Inspection 982504 — Indena S.P.A.

Indena S.P.A. — FEI 1000280888

The FDA completed an inspection of Indena S.P.A. on Jul 29, 2016 in Settala. 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
Jul 29, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Settala (Italy)