FDA Inspection 1088856 — Patheon Inc.

Patheon Inc. — FEI 3000264888

The FDA completed an inspection of Patheon Inc. on April 12, 2019 in Mississauga. 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 12, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mississauga (Canada)