# Confab Laboratories Inc. - Inspection Records

Source: https://www.keypedia.com/companies/confab-laboratories-inc/cae88900-5d2c-47b7-aedc-3931dd4f8310

> Inspection records and compliance data for Confab Laboratories Inc. in Saint-Hubert, None. Access full analysis and detailed observations.

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## Details

- Name: Confab Laboratories Inc.
- FEI Number: 3000198340
- Canada Business Number: 839826401RC0002
- City: Saint-Hubert
- State: None
- Country Name: Canada
- Address Line 1: 4355 Sir-Wilfrid-Laurier Blvd
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK, REPACK

## Related Documents

- [Canada Inspection - Confab Laboratories Inc. - Inspection #87288 - 2025-09-03](https://www.keypedia.com/records/canada_inspection/confab-laboratories-inc/a80f86a3-f057-4a5f-9e10-efc71acf5024) — source: Canada, date: September 3, 2025
- [FDA Inspection 1254270 - Confab Laboratories Inc. - 2025-02-21](https://www.keypedia.com/records/fda_inspections/confab-laboratories-inc/ea77c99a-60f3-4612-a8e4-1f998145330e) — source: FDA, date: February 21, 2025
- [FDA Inspection 1254270 - Confab Laboratories Inc. - 2025-02-21](https://www.keypedia.com/records/fda_inspections/confab-laboratories-inc/78eed15d-bcbc-48d9-ae2d-b3335ba4531b) — classification: No Action Indicated (NAI), source: FDA, date: February 21, 2025
- [FDA Inspection 1254270 - Confab Laboratories Inc. - 2025-02-21](https://www.keypedia.com/records/fda_inspections/confab-laboratories-inc/f49d3fad-4955-4d7f-ac0d-8e8c6b023705) — classification: No Action Indicated (NAI), source: FDA, date: February 21, 2025
- [FDA Inspection 1199219 - Confab Laboratories Inc. - 2023-02-03](https://www.keypedia.com/records/fda_inspections/confab-laboratories-inc/75a461ad-065b-4fbe-8499-00e927096407) — classification: No Action Indicated (NAI), source: FDA, date: February 3, 2023
- [Canada Inspection - Confab Laboratories Inc. - Inspection #79397 - 2022-09-14](https://www.keypedia.com/records/canada_inspection/confab-laboratories-inc/25bbebf8-ce89-4764-af0e-33dd5a750a04) — source: Canada, date: September 14, 2022
- [Canada Inspection - Confab Laboratories Inc. - Inspection #73587 - 2020-01-28](https://www.keypedia.com/records/canada_inspection/confab-laboratories-inc/09f88227-78ca-46a0-a959-7332f5f24b4d) — source: Canada, date: January 28, 2020
- [Canada Inspection - Confab Laboratories Inc. - Inspection #69650 - 2018-03-19](https://www.keypedia.com/records/canada_inspection/confab-laboratories-inc/5562afac-09ad-407a-a35e-82582b366d4e) — source: Canada, date: March 19, 2018
- [FDA Inspection 1032527 - Confab Laboratories Inc. - 2017-12-01](https://www.keypedia.com/records/fda_inspections/confab-laboratories-inc/9d899412-88b7-4c78-b563-984f2b9f34dd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 1, 2017
- [FDA Inspection 948793 - Confab Laboratories Inc. - 2015-10-30](https://www.keypedia.com/records/fda_inspections/confab-laboratories-inc/1f93203a-c15c-4d34-824c-8483d69a19eb) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2015
- [FDA Inspection 906516 - Confab Laboratories Inc. - 2014-10-24](https://www.keypedia.com/records/fda_inspections/confab-laboratories-inc/c7733032-6fbc-4943-9f22-f44bf0c67cfe) — classification: No Action Indicated (NAI), source: FDA, date: October 24, 2014
- [FDA Inspection 840459 - Confab Laboratories Inc. - 2013-06-07](https://www.keypedia.com/records/fda_inspections/confab-laboratories-inc/c0a91bb8-7b56-43a7-92ce-4d678f544a26) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 7, 2013
- [FDA Inspection 840459 - Confab Laboratories Inc. - 2013-06-07](https://www.keypedia.com/records/fda_inspections/confab-laboratories-inc/0212de35-44cc-4af9-b587-6a10639968e6) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2013
- [FDA Inspection 748324 - Confab Laboratories Inc. - 2011-09-29](https://www.keypedia.com/records/fda_inspections/confab-laboratories-inc/300e19df-74c5-4d92-8399-83d5567e5942) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 29, 2011

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