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Kesair Technologies, LLC FDA Record

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

Latest inspection VAI · Feb 3, 2020
No warning letters matched by name

Inspections 5

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 0 None on file

Kesair Technologies, LLC has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Kesair Technologies, LLC" is on file.

What these totals cover: FDA records filed under the name "Kesair Technologies, LLC" and its spelling variant "Kesair Technologies".

Latest inspection: Feb 3, 2020 · 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	5	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

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

Kesair Technologies, LLC: FDA inspections per year

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	0	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	1	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.

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Recent FDA inspections

5 inspections from Jul 15, 2009 to Feb 3, 2020.

Date	Site	Product	Classification	FEI
Feb 3, 2020	Kennesaw, GA	Devices	Voluntary Action Indicated (VAI)	3002959861
Feb 15, 2017	Kennesaw, GA	Devices	No Action Indicated (NAI)	3002959861
Feb 26, 2014	Kennesaw, GA	Devices	No Action Indicated (NAI)	3002959861
Feb 9, 2011	Kennesaw, GA	Devices	Voluntary Action Indicated (VAI)	3002959861
Jul 15, 2009	Kennesaw, GA	Devices	Voluntary Action Indicated (VAI)	3002959861

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 3002959861	Kennesaw, GA	5	Feb 3, 2020

Kesair Technologies, LLC and the FDA: common questions

Has Kesair Technologies, LLC received an FDA warning letter?

No FDA warning letter addressed to the name "Kesair Technologies, LLC" 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 Kesair Technologies, LLC received an FDA Form 483?

FDA has not published a Form 483 for "Kesair Technologies, LLC" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Kesair Technologies, LLC?

The most recent FDA inspection on file ended Feb 3, 2020 at Kennesaw, GA and was classified VAI. FDA has 5 inspections of Kesair Technologies, LLC on file.

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