FDA Inspection 877083 — Patheon Italia S.P.A.

Patheon Italia S.P.A. — FEI 3003065803

The FDA completed an inspection of Patheon Italia S.P.A. on Apr 8, 2014 in Monza. 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
Apr 8, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Monza (Italy)

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