FDA Inspection 1194792 — Apotex Inc.

Apotex Inc. — FEI 3000114091

The FDA completed an inspection of Apotex Inc. on December 16, 2022 in Brantford. 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
December 16, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brantford (Canada)