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K & K Distribution, Inc.

FDA Regulatory Profile

K & K Distribution, Inc. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Mar 24, 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
Inspections4Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 24, 2026Holmen, WIFood/CosmeticsNo Action Indicated (NAI)3044469737
Jul 26, 2022Glendale, CAFood/CosmeticsOfficial Action Indicated (OAI)3017875108
Dec 3, 2020Glendale, CAFood/CosmeticsOfficial Action Indicated (OAI)3017875108
Feb 27, 2019Glendale, CAFood/CosmeticsVoluntary Action Indicated (VAI)3017875108

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 3044469737Holmen, WI1Mar 24, 2026
FEI 3017875108Glendale, CA3Jul 26, 2022

FDA data resources

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