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Kesair Technologies, LLC FDA Inspection Record

FEI 3002959861 · Inspections, Form 483s, warning letters and import refusals

Kesair Technologies, LLC is an FDA-inspected facility (FEI 3002959861) located in Kennesaw, GA, US. RegDataLab tracks 5 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Feb 3, 2020: Voluntary Action Indicated (VAI)
Inspections on record
5 (3 VAI, 2 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Feb 3, 2020Voluntary Action Indicated (VAI)Procedures not adequately established or maintained (21 CFR 820.40)
Quality audits - Lack of or inadequate procedures (21 CFR 820.22)
Training - Lack of or inadequate procedures (21 CFR 820.25(b))
Design history file (21 CFR 820.30(j))
and 5 more
Feb 15, 2017No Action Indicated (NAI)No citations listed
Feb 26, 2014No Action Indicated (NAI)No citations listed
Feb 9, 2011Voluntary Action Indicated (VAI)Lack of or inadequate final acceptance procedures (21 CFR 820.80(d))
Documentation (21 CFR 820.80(e))
Jul 15, 2009Voluntary Action Indicated (VAI)Document review, approval documentation (21 CFR 820.40(a))
Procedures (21 CFR 820.100(b))
Documentation (21 CFR 820.100(b))
Training records (21 CFR 820.25(b))
and 1 more

FDA record score

2 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 14, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

3 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAIFeb 3, 20206 x 0.251.5
Inspection classified VAIFeb 9, 201110 years or older, so it adds no points0
Inspection classified VAIJul 15, 200910 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Kesair Technologies, LLC
Location
Kennesaw, GA (US)
Source
inspections

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.