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 — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 19, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ferentino (Italy)