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Universal Pure, LLC

FDA Regulatory Profile

Universal Pure, LLC has 0 FDA recalls, 12 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jul 29, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections12Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 29, 2026Jurupa Valley, CAFood/CosmeticsNo Action Indicated (NAI)3020996583
Jun 23, 2025Lincoln, NEFood/CosmeticsNo Action Indicated (NAI)3004804570
Jan 8, 2025Lincoln, NEFood/CosmeticsNo Action Indicated (NAI)3004804570
Dec 11, 2024Malvern, PAFood/CosmeticsNo Action Indicated (NAI)3011369235
Apr 21, 2023Jurupa Valley, CAFood/CosmeticsNo Action Indicated (NAI)3020996583
Jul 21, 2020Meriden, CTFood/CosmeticsVoluntary Action Indicated (VAI)3009841929
Aug 14, 2019Meriden, CTFood/CosmeticsVoluntary Action Indicated (VAI)3009841929
Mar 27, 2019Malvern, PAFood/CosmeticsNo Action Indicated (NAI)3011369235
Aug 3, 2017Meriden, CTFood/CosmeticsVoluntary Action Indicated (VAI)3009841929
Aug 12, 2016Meriden, CTFood/CosmeticsOfficial Action Indicated (OAI)3009841929
Dec 16, 2015Lincoln, NEVeterinaryNo Action Indicated (NAI)3004804570
Jun 20, 2013Meriden, CTVeterinaryNo Action Indicated (NAI)3009841929

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 3020996583Jurupa Valley, CA2Jul 29, 2026
FEI 3004804570Lincoln, NE3Jun 23, 2025
FEI 3011369235Malvern, PA2Dec 11, 2024
FEI 3009841929Meriden, CT5Jul 21, 2020

FDA data resources

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