FDA Inspection 1072831 — Indena S.P.A.

Indena S.P.A. — FEI 1000280888

The FDA completed an inspection of Indena S.P.A. on May 10, 2018 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
May 10, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Settala (Italy)

Additional Details

Mutual Recognition Agreement (MRA)