Ben E. Keith Company

FDA Regulatory Profile

Ben E. Keith Company has 0 FDA recalls, 11 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 6, 2026 · 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
Inspections11Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 6, 2026Edmond, OKFood/CosmeticsNo Action Indicated (NAI)1622103
Apr 1, 2026Gainesville, FLFood/CosmeticsNo Action Indicated (NAI)1013938
Aug 29, 2025Amarillo, TXFood/CosmeticsNo Action Indicated (NAI)2000034678
Jul 15, 2022Albuquerque, NMFood/CosmeticsNo Action Indicated (NAI)3004300861
Jun 21, 2019Edmond, OKFood/CosmeticsNo Action Indicated (NAI)1622103
Jan 11, 2017Dodge City, KSFood/CosmeticsNo Action Indicated (NAI)1920143
Apr 17, 2015Abilene, TXFood/CosmeticsNo Action Indicated (NAI)1616083
May 7, 2014Edmond, OKFood/CosmeticsVoluntary Action Indicated (VAI)1622103
Feb 24, 2014Abilene, TXFood/CosmeticsNo Action Indicated (NAI)1616083
Jul 30, 2012Edmond, OKFood/CosmeticsNo Action Indicated (NAI)1622103
Jun 21, 2010Amarillo, TXFood/CosmeticsNo Action Indicated (NAI)2000034678

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 1622103Edmond, OK4May 6, 2026
FEI 1013938Gainesville, FL1Apr 1, 2026
FEI 2000034678Amarillo, TX2Aug 29, 2025
FEI 3004300861Albuquerque, NM1Jul 15, 2022
FEI 1920143Dodge City, KS1Jan 11, 2017
FEI 1616083Abilene, TX2Apr 17, 2015

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