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Fulex, LLC

FDA Regulatory Profile

Fulex, LLC has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 5, 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 actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 5, 2026Poway, CAFood/CosmeticsNo Action Indicated (NAI)3016789201
Dec 17, 2025Warren, MIFood/CosmeticsNo Action Indicated (NAI)2000015568
Mar 25, 2025Chattanooga, TNFood/CosmeticsVoluntary Action Indicated (VAI)3019867798
Sep 10, 2021Warren, MIFood/CosmeticsNo Action Indicated (NAI)2000015568

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 3016789201Poway, CA1Aug 5, 2026
FEI 2000015568Warren, MI2Dec 17, 2025
FEI 3019867798Chattanooga, TN1Mar 25, 2025

FDA data resources

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