FDA Inspection 762598 — Patheon Italia S.p.A

Patheon Italia S.p.A — FEI 3004110157

The FDA completed an inspection of Patheon Italia S.p.A on November 11, 2011 in Ferentino. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 11, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ferentino (Italy)