FDA Inspection 1066263 — Patheon Italia S.P.A

Patheon Italia S.P.A — FEI 3004110157

The FDA completed an inspection of Patheon Italia S.P.A on Sep 21, 2018 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
Sep 21, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ferentino (Italy)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.