Home / Companies / ID Biomedical Corporation Of Quebec

ID Biomedical Corporation Of Quebec FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Latest inspection NAI · Mar 28, 2025
Last warning letter 2014

Inspections 8

1 OAI

Recalls 0 0 Class I

Warning letters 1 Latest Jun 12, 2014

510(k) clearances 0 None on file

ID Biomedical Corporation Of Quebec has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to ID Biomedical Corporation Of Quebec, the most recent on Jun 12, 2014. FDA has published 1 Form 483 for ID Biomedical Corporation Of Quebec.

What these totals cover: FDA records filed under the name "ID Biomedical Corporation Of Quebec".

Latest inspection: Mar 28, 2025 · NAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 11, 2026 (checked Nov 15, 2026, unchanged)	File dated Nov 10, 2026	Current
510(k) clearances	0	Nov 15, 2026	File dated Nov 9, 2026	Current
Inspections	8	Nov 15, 2026	Newest record Nov 5, 2026	Current
Compliance actions	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

ID Biomedical Corporation Of Quebec's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

ID Biomedical Corporation Of Quebec: FDA inspections per year

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	0	0	0	0	0
2022	1	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.

Reviewing ID Biomedical Corporation Of Quebec as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check ID Biomedical Corporation Of Quebec yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

ID Biomedical Corporation Of Quebec FDA Warning Letters

1 warning letter on Jun 12, 2014.

Issued	Subject	Issuing office	Close-out letter
Jun 12, 2014 · Record page

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

ID Biomedical Corporation Of Quebec Form 483s

1 Form 483 published by FDA.

Date	Document	FEI
May 20, 2022 · Document on fda.gov	483	3004835647

A Form 483 lists the observations FDA investigators made at the end of an inspection. FDA publishes some Form 483s in its reading room, and each date links to that document. Read the observations with the FDA 483 search.

Recent FDA inspections

8 inspections from May 28, 2009 to Mar 28, 2025.

Date	Site	Product	Classification	FEI
Mar 28, 2025	Quebec, Canada	Biologics	No Action Indicated (NAI)	3004835647
May 20, 2022	Quebec, Canada	Biologics	Voluntary Action Indicated (VAI)	3004835647
May 26, 2017	Quebec, Canada	Biologics	Voluntary Action Indicated (VAI)	3004835647
Jun 5, 2015	Quebec, Canada	Biologics	Voluntary Action Indicated (VAI)	3004835647
Apr 9, 2014	Quebec, Canada	Biologics	Official Action Indicated (OAI)	3004835647
Apr 7, 2011	Quebec, Canada	Biologics	Voluntary Action Indicated (VAI)	3004835647
Mar 16, 2010	Quebec, Canada	Biologics	Voluntary Action Indicated (VAI)	3004835647
May 28, 2009	Quebec, Canada	Biologics	Voluntary Action Indicated (VAI)	3004835647

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.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under ID Biomedical Corporation Of Quebec: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Jun 12, 2014.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3004835647	Quebec, Canada	8	Mar 28, 2025

ID Biomedical Corporation Of Quebec and the FDA: common questions

Has ID Biomedical Corporation Of Quebec received an FDA warning letter?

Yes. FDA has issued 1 warning letter to ID Biomedical Corporation Of Quebec. The most recent is dated Jun 12, 2014.

Has ID Biomedical Corporation Of Quebec received an FDA Form 483?

FDA has published 1 Form 483 for ID Biomedical Corporation Of Quebec in its reading room, the most recent dated May 20, 2022. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect ID Biomedical Corporation Of Quebec?

The most recent FDA inspection on file ended Mar 28, 2025 at Quebec, Canada and was classified NAI. FDA has 8 inspections of ID Biomedical Corporation Of Quebec on file, 1 of them classified OAI (official action indicated).

Need more than this page shows? Ask about ID Biomedical Corporation Of Quebec in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.