FDA Inspection 926682 — Patheon Italia S.P.A

Patheon Italia S.P.A — FEI 3004110157

The FDA completed an inspection of Patheon Italia S.P.A on May 19, 2015 in Ferentino. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
May 19, 2015
Fiscal Year
2015
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.