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NEXAIR, LLC

FDA Regulatory Profile

NEXAIR, LLC has 0 FDA recalls, 35 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 16, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections35Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 16, 2025North Little Rock, ARFood/CosmeticsNo Action Indicated (NAI)2314309
Dec 11, 2024Little Rock, ARFood/CosmeticsNo Action Indicated (NAI)3009891431
Jul 11, 2024Jacksonville, FLDrugsVoluntary Action Indicated (VAI)1015040
Jan 12, 2024Okeechobee, FLDrugsVoluntary Action Indicated (VAI)1036503
Dec 6, 2023Orlando, FLDrugsNo Action Indicated (NAI)1038820
Nov 23, 2021Fairburn, GADrugsNo Action Indicated (NAI)1039095
Sep 10, 2019Fairburn, GADevicesNo Action Indicated (NAI)1039095
Mar 22, 2019Norcross, GADrugsNo Action Indicated (NAI)3009907525
Aug 1, 2018Okeechobee, FLFood/CosmeticsVoluntary Action Indicated (VAI)1036503
Mar 6, 2018Monroe, LADrugsNo Action Indicated (NAI)2311255
Feb 27, 2018Alexandria, LADrugsNo Action Indicated (NAI)2318101
Feb 5, 2018Jacksonville, FLFood/CosmeticsNo Action Indicated (NAI)1015040
Sep 3, 2015Knoxville, TNDrugsNo Action Indicated (NAI)3003972398
Aug 18, 2015Cave City, KYDrugsNo Action Indicated (NAI)3006854582
Feb 27, 2015North Little Rock, ARDrugsVoluntary Action Indicated (VAI)2314309
Aug 25, 2014Fairburn, GADrugsNo Action Indicated (NAI)1039095
Aug 12, 2014Memphis, TNDrugsNo Action Indicated (NAI)1020303
Jun 11, 2013Tallahassee, FLDrugsNo Action Indicated (NAI)1047172
Apr 17, 2013Huntsville, ALDrugsNo Action Indicated (NAI)3000206647
Mar 26, 2013Okeechobee, FLFood/CosmeticsNo Action Indicated (NAI)1036503

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 2314309North Little Rock, AR2Dec 16, 2025
FEI 3009891431Little Rock, AR1Dec 11, 2024
FEI 1015040Jacksonville, FL4Jul 11, 2024
FEI 1036503Okeechobee, FL3Jan 12, 2024
FEI 1038820Orlando, FL2Dec 6, 2023
FEI 1039095Fairburn, GA3Nov 23, 2021
FEI 3009907525Norcross, GA1Mar 22, 2019
FEI 2311255Monroe, LA1Mar 6, 2018
FEI 2318101Alexandria, LA1Feb 27, 2018
FEI 3003972398Knoxville, TN1Sep 3, 2015
FEI 3006854582Cave City, KY1Aug 18, 2015
FEI 1020303Memphis, TN4Aug 12, 2014
FEI 1047172Tallahassee, FL1Jun 11, 2013
FEI 3000206647Huntsville, AL1Apr 17, 2013
FEI 3005011025Memphis, TN2Jan 23, 2012
FEI 1000525131Columbia, TN1Jan 5, 2012
FEI 3004909308Madison, TN1Dec 21, 2011
FEI 3004881907Sarasota, FL1Apr 13, 2011
FEI 1000307515Nashville, TN1Apr 6, 2011
FEI 3002986495Norcross, GA1Jul 14, 2010
FEI 3003868427Pearl, MS1Jul 7, 2010
FEI 3003329108Jacksonville, FL1Feb 25, 2010

FDA data resources

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