# Apotex, Inc., Etobicoke, Canada – FDA Inspections

Source: https://www.keypedia.com/companies/apotex-inc/3fb3d66a-fef9-4c47-82b5-da446ecf3593

> Inspection records and compliance data for Apotex, Inc. in Etobicoke. 9 FDA inspections on record (1 OAI), 1 Form 483, last inspected September 27, 2024.

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## Details

- Name: Apotex, Inc.
- FEI Number: 3002808376
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE
- Address Line 1: 50 Steinway Blvd
- City: Etobicoke
- Country Name: Canada
- Address: 50 Steinway Blvd, Etobicoke, Canada
- Country: Canada

## Related Documents

- FDA Inspection 1249246 - Apotex, Inc. - 2024-09-27 — source: FDA, date: September 27, 2024
- FDA Inspection 1249246 - Apotex, Inc. - 2024-09-27 — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2024
- FDA Inspection 1230073 - Apotex, Inc. - 2024-02-23 — classification: No Action Indicated (NAI), source: FDA, date: February 23, 2024
- FDA Inspection 1114893 - Apotex, Inc. - 2019-11-08 — classification: No Action Indicated (NAI), source: FDA, date: November 8, 2019
- [FDA Inspection 1100432 - Apotex, Inc. - 2019-07-12](https://www.keypedia.com/records/fda_inspections/apotex-inc/8f560e23-4ace-4769-92c5-5cf425bcfb61) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2019
- FDA Inspection 1035875 - Apotex, Inc. - 2017-12-08 — classification: No Action Indicated (NAI), source: FDA, date: December 8, 2017
- FDA Inspection 982370 - Apotex, Inc. - 2016-05-27 — classification: No Action Indicated (NAI), source: FDA, date: May 27, 2016
- FDA Inspection 850692 - Apotex, Inc. - 2013-09-13 — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2013
- FDA Inspection 714923 - Apotex, Inc. - 2011-02-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 11, 2011
- [FDA Inspection 554921 - Apotex, Inc. - 2008-12-19](https://www.keypedia.com/records/fda_inspections/apotex-inc/8377a1ed-7ef2-4ec0-8795-5ea9fd958f48) — classification: Official Action Indicated (OAI), source: FDA, date: December 19, 2008

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