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Luce Enterprises LLC

FDA Regulatory Profile

Luce Enterprises LLC has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Aug 5, 2026 · OAI

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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 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 5, 2026Mcallen, TXFood/CosmeticsOfficial Action Indicated (OAI)3015433591
May 17, 2023Mcallen, TXFood/CosmeticsVoluntary Action Indicated (VAI)3015433591
Jul 28, 2022Mcallen, TXFood/CosmeticsOfficial Action Indicated (OAI)3015433591
Apr 23, 2020Mcallen, TXFood/CosmeticsVoluntary Action Indicated (VAI)3015433591

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 3015433591Mcallen, TX4Aug 5, 2026

FDA data resources

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