FDA Inspection 1247104 — Patheon Italia S.P.A

Patheon Italia S.P.A — FEI 3004110157

The FDA completed an inspection of Patheon Italia S.P.A on Feb 25, 2022 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
Feb 25, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ferentino (Italy)

Additional Details

Mutual Recognition Agreement (MRA)

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