FDA Inspection 1095165 — Apotex Inc.

Apotex Inc. — FEI 3000114091

The FDA completed an inspection of Apotex Inc. on May 24, 2019 in Brantford. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 24, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brantford (Canada)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.