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Oklahoma Blood Institute FDA Record

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

Oklahoma Blood Institute has 0 FDA recalls, 37 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Oklahoma Blood Institute" is on file.

What these totals cover: FDA records filed under the name "Oklahoma Blood Institute".

Latest inspection: Aug 26, 2026 · VAI

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	37	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

Oklahoma Blood Institute'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	1	0	0	0	0
2025	3	0	0	0	0
2024	1	0	0	0	0
2023	1	0	0	0	0
2022	2	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	1	0	0	0	0
2018	3	0	0	0	0
2017	2	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

37 inspections from Aug 7, 2009 to Aug 26, 2026. Showing the 20 most recent. View all 37 inspections

Date	Site	Product	Classification	FEI
Aug 26, 2026	Tulsa, OK	Biologics	Voluntary Action Indicated (VAI)	3003949970
Jul 23, 2025	Hot Springs, AR	Biologics	No Action Indicated (NAI)	3008629223
May 1, 2025	Fort Smith, AR	Biologics	No Action Indicated (NAI)	3008629186
Feb 6, 2025	Little Rock, AR	Biologics	No Action Indicated (NAI)	3011714312
Aug 20, 2024	Oklahoma City, OK	Biologics	No Action Indicated (NAI)	1626009
Feb 3, 2023	Hot Springs, AR	Biologics	No Action Indicated (NAI)	3008629223
Apr 28, 2022	Little Rock, AR	Biologics	No Action Indicated (NAI)	3011714312
Feb 16, 2022	Fort Smith, AR	Biologics	No Action Indicated (NAI)	3008629186
Jun 7, 2019	Oklahoma City, OK	Biologics	Voluntary Action Indicated (VAI)	1626009
Aug 30, 2018	Hot Springs, AR	Biologics	No Action Indicated (NAI)	3008629223
Jul 20, 2018	Little Rock, AR	Biologics	Voluntary Action Indicated (VAI)	3011714312
Apr 4, 2018	Fort Smith, AR	Biologics	No Action Indicated (NAI)	3008629186
Dec 7, 2017	Tulsa, OK	Biologics	No Action Indicated (NAI)	3003949970
Jun 20, 2017	Oklahoma City, OK	Biologics	No Action Indicated (NAI)	1626009
Oct 19, 2016	Little Rock, AR	Biologics	No Action Indicated (NAI)	3011714312
Aug 2, 2016	Hot Springs, AR	Biologics	No Action Indicated (NAI)	3008629223
Mar 24, 2016	Fort Smith, AR	Biologics	No Action Indicated (NAI)	3008629186
Oct 16, 2015	Tulsa, OK	Biologics	Voluntary Action Indicated (VAI)	3003949970
Oct 6, 2015	Little Rock, AR	Biologics	No Action Indicated (NAI)	3011714312
Aug 20, 2015	Oklahoma City, OK	Biologics	Voluntary Action Indicated (VAI)	1626009

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

6 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3003949970	Tulsa, OK	5	Aug 26, 2026
FEI 3008629223	Hot Springs, AR	8	Jul 23, 2025
FEI 3008629186	Fort Smith, AR	8	May 1, 2025
FEI 3011714312	Little Rock, AR	5	Feb 6, 2025
FEI 1626009	Oklahoma City, OK	8	Aug 20, 2024
FEI 3000204268	Ponca City, OK	3	Mar 1, 2013

Oklahoma Blood Institute and the FDA: common questions

Has Oklahoma Blood Institute received an FDA warning letter?

No FDA warning letter addressed to the name "Oklahoma Blood Institute" 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 Oklahoma Blood Institute received an FDA Form 483?

FDA has not published a Form 483 for "Oklahoma Blood Institute" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Oklahoma Blood Institute?

The most recent FDA inspection on file ended Aug 26, 2026 at Tulsa, OK and was classified VAI. FDA has 37 inspections of Oklahoma Blood Institute on file.

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