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Furst-McNess Company

FDA Regulatory Profile

Furst-McNess Company has 0 FDA recalls, 23 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Aug 21, 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
Inspections23Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 21, 2025Lodi, WIVeterinaryNo Action Indicated (NAI)3003426240
Jul 2, 2025Live Oak, FLVeterinaryVoluntary Action Indicated (VAI)3033412493
Apr 29, 2025Lake City, FLVeterinaryNo Action Indicated (NAI)3002787852
Aug 1, 2024Lodi, WIVeterinaryOfficial Action Indicated (OAI)3003426240
May 31, 2024Lake City, FLVeterinaryVoluntary Action Indicated (VAI)3002787852
Aug 28, 2023Lodi, WIVeterinaryOfficial Action Indicated (OAI)3003426240
Mar 6, 2023Seneca, WIVeterinaryNo Action Indicated (NAI)3003506190
Nov 12, 2021Lodi, WIVeterinaryVoluntary Action Indicated (VAI)3003426240
Mar 12, 2020Gering, NEVeterinaryNo Action Indicated (NAI)1922249
Nov 13, 2019Lodi, WIVeterinaryNo Action Indicated (NAI)3003426240
Sep 17, 2019Lake City, FLVeterinaryNo Action Indicated (NAI)3002787852
Aug 28, 2018Montezuma, GAVeterinaryNo Action Indicated (NAI)3008885950
May 24, 2018Gering, NEVeterinaryVoluntary Action Indicated (VAI)1922249
Dec 5, 2017Lodi, WIVeterinaryNo Action Indicated (NAI)3003426240
May 26, 2017Gering, NEVeterinaryOfficial Action Indicated (OAI)1922249
Sep 22, 2016Gering, NEVeterinaryVoluntary Action Indicated (VAI)1922249
Aug 24, 2015Lake City, FLVeterinaryNo Action Indicated (NAI)3002787852
Jul 11, 2013Cordele, GAVeterinaryNo Action Indicated (NAI)3004338613
May 17, 2011Freeport, ILFood/CosmeticsNo Action Indicated (NAI)1410488
May 17, 2011Eleroy, ILVeterinaryNo Action Indicated (NAI)3004339715

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 3003426240Lodi, WI8Aug 21, 2025
FEI 3033412493Live Oak, FL1Jul 2, 2025
FEI 3002787852Lake City, FL5Apr 29, 2025
FEI 3003506190Seneca, WI1Mar 6, 2023
FEI 1922249Gering, NE4Mar 12, 2020
FEI 3008885950Montezuma, GA1Aug 28, 2018
FEI 3004338613Cordele, GA1Jul 11, 2013
FEI 1410488Freeport, IL1May 17, 2011
FEI 3004339715Eleroy, IL1May 17, 2011

FDA data resources

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