FDA Inspection 1206091 — Patheon Italia S.p.A.

Patheon Italia S.p.A. — FEI 3003065803

The FDA completed an inspection of Patheon Italia S.p.A. on April 8, 2022 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
April 8, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Monza (Italy)

Additional Details

Mutual Recognition Agreement (MRA)