# Eurofins CDMO Alphora Inc. - Inspection Records

Source: https://www.keypedia.com/companies/eurofins-cdmo-alphora-inc/0a1af317-8d90-4723-be66-a19dc7fa04b7

> Inspection records and compliance data for Eurofins CDMO Alphora Inc. in Mississauga. 5 FDA inspections on record, 1 Form 483, last inspected January 17, 2025.

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## Details

- Name: Eurofins CDMO Alphora Inc.
- FEI Number: 3005804912
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING
- Address Line 1: 2395 Speakman Dr Suite 2001
- City: Mississauga
- Country Name: Canada
- Address: 2395 Speakman Dr Suite 2001, Mississauga, Canada
- Country: Canada

## Related Documents

- [FDA Inspection 1258608 - Eurofins CDMO Alphora Inc. - 2025-01-17](https://www.keypedia.com/records/fda_inspections/eurofins-cdmo-alphora-inc/0a16cbc4-1d92-487d-86c5-f93412aa7e66) — source: FDA, date: January 17, 2025
- FDA Inspection 1258608 - Eurofins CDMO Alphora Inc. - 2025-01-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 17, 2025
- FDA Inspection 1106349 - Eurofins CDMO Alphora Inc. - 2019-10-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 11, 2019
- [FDA Inspection 972749 - Eurofins CDMO Alphora Inc. - 2016-04-29](https://www.keypedia.com/records/fda_inspections/eurofins-cdmo-alphora-inc/3948f06b-18b1-443f-ad06-9f850cb9bffd) — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2016
- [FDA Inspection 870592 - Eurofins CDMO Alphora Inc. - 2014-02-20](https://www.keypedia.com/records/fda_inspections/eurofins-cdmo-alphora-inc/a50f8b9f-75bb-4623-9f50-254a905da4c3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 20, 2014
- FDA Inspection 757080 - Eurofins CDMO Alphora Inc. - 2011-12-02 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 2, 2011

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