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Sanford Health IRB FDA Record

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

Latest inspection NAI · Aug 11, 2025
No warning letters matched by name

Inspections 4

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 0 None on file

Sanford Health IRB has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Sanford Health IRB" is on file.

What these totals cover: FDA records filed under the name "Sanford Health IRB".

Latest inspection: Aug 11, 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	4	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

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

Sanford Health IRB: 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	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

4 inspections from Jan 18, 2011 to Aug 11, 2025.

Date	Site	Product	Classification	FEI
Aug 11, 2025	Sioux Falls, SD	Devices	No Action Indicated (NAI)	3008660749
May 18, 2018	Sioux Falls, SD	Drugs	No Action Indicated (NAI)	3008660749
Mar 8, 2013	Sioux Falls, SD	Drugs	No Action Indicated (NAI)	3008660749
Jan 18, 2011	Sioux Falls, SD	Drugs	Voluntary Action Indicated (VAI)	3008660749

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 3008660749	Sioux Falls, SD	4	Aug 11, 2025

Sanford Health IRB and the FDA: common questions

Has Sanford Health IRB received an FDA warning letter?

No FDA warning letter addressed to the name "Sanford Health 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 Sanford Health IRB received an FDA Form 483?

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

When did the FDA last inspect Sanford Health IRB?

The most recent FDA inspection on file ended Aug 11, 2025 at Sioux Falls, SD and was classified NAI. FDA has 4 inspections of Sanford Health IRB on file.

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