FDA Inspection 733806 — Patheon Italia S.p.A.

Patheon Italia S.p.A. — FEI 3003065803

The FDA completed an inspection of Patheon Italia S.p.A. on June 21, 2011 in Monza. 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
June 21, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Monza (Italy)