FDA Inspection 955569 — Patheon Italia S.P.A

Patheon Italia S.P.A — FEI 3004110157

The FDA completed an inspection of Patheon Italia S.P.A on Dec 16, 2015 in Ferentino. 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
Dec 16, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ferentino (Italy)

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