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Confab Laboratories Inc.

FDA Regulatory Profile

Confab Laboratories Inc. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Confab Laboratories Inc." and its spelling variant "Confab Laboratories".

Latest inspection: Feb 21, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	8	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Confab Laboratories Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	1	0	0	0	0
2024	0	0	0	0	0
2023	1	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	0	0	0	0	0
2018	0	0	0	0	0
2017	1	0	0	0	0

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA inspections

8 inspections from Apr 8, 2009 to Feb 21, 2025.

Date	Site	Product	Classification	FEI
Feb 21, 2025	Saint-Hubert, Canada	Food/Cosmetics	No Action Indicated (NAI)	3000198340
Feb 3, 2023	Saint-Hubert, Canada	Drugs	No Action Indicated (NAI)	3000198340
Dec 1, 2017	Saint-Hubert, Canada	Drugs	Voluntary Action Indicated (VAI)	3000198340
Oct 30, 2015	Saint-Hubert, Canada	Drugs	No Action Indicated (NAI)	3000198340
Oct 24, 2014	Saint-Hubert, Canada	Drugs	No Action Indicated (NAI)	3000198340
Jun 7, 2013	Saint-Hubert, Canada	Veterinary	No Action Indicated (NAI)	3000198340
Sep 29, 2011	Saint-Hubert, Canada	Drugs	Voluntary Action Indicated (VAI)	3000198340
Apr 8, 2009	Saint-Hubert, Canada	Drugs	Voluntary Action Indicated (VAI)	3000198340

NAI: No objectionable conditions or practices were found during the inspection.
VAI: Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI: Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3000198340	Saint-Hubert, Canada	8	Feb 21, 2025

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