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St. Louis University IRB FDA Record

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

St. Louis University IRB has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "St. Louis University IRB" is on file.

What these totals cover: FDA records filed under the name "St. Louis University IRB".

Latest inspection: Mar 20, 2025 · NAI

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	3	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

St. Louis University IRB'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	0	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	1	0	0	0	0
2017	0	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.

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Recent FDA inspections

3 inspections from Dec 9, 2010 to Mar 20, 2025.

Date	Site	Product	Classification	FEI
Mar 20, 2025	Saint Louis, MO	Devices	No Action Indicated (NAI)	1926213
Feb 27, 2018	Saint Louis, MO	Drugs	No Action Indicated (NAI)	1926213
Dec 9, 2010	Saint Louis, MO	Devices	No Action Indicated (NAI)	1926213

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 1926213	Saint Louis, MO	3	Mar 20, 2025

St. Louis University IRB and the FDA: common questions

Has St. Louis University IRB received an FDA warning letter?

No FDA warning letter addressed to the name "St. Louis University IRB" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has St. Louis University IRB received an FDA Form 483?

FDA has not published a Form 483 for "St. Louis University IRB" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect St. Louis University IRB?

The most recent FDA inspection on file ended Mar 20, 2025 at Saint Louis, MO and was classified NAI. FDA has 3 inspections of St. Louis University IRB on file.

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