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Kepix, Corp.

FDA Regulatory Profile

Kepix, Corp. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 1, 2026 · VAI

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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
Inspections5Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 1, 2026Doral, FLFood/CosmeticsVoluntary Action Indicated (VAI)3012399973
Jan 31, 2023Doral, FLFood/CosmeticsOfficial Action Indicated (OAI)3012399973
Feb 28, 2022Doral, FLFood/CosmeticsVoluntary Action Indicated (VAI)3012399973
Aug 22, 2019Doral, FLFood/CosmeticsVoluntary Action Indicated (VAI)3012399973
Aug 31, 2017Doral, FLFood/CosmeticsVoluntary Action Indicated (VAI)3012399973

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 3012399973Doral, FL5Jun 1, 2026

FDA data resources

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