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Langer Juice Company, Inc.

FDA Regulatory Profile

Langer Juice Company, Inc. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jan 27, 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
Inspections8Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 27, 2026City Of Industry, CAFood/CosmeticsNo Action Indicated (NAI)2016539
Jul 31, 2025City Of Industry, CAFood/CosmeticsNo Action Indicated (NAI)2016539
Feb 10, 2023City Of Industry, CAFood/CosmeticsNo Action Indicated (NAI)2016539
Jul 16, 2018City Of Industry, CAFood/CosmeticsNo Action Indicated (NAI)2016539
Jun 16, 2015City Of Industry, CAFood/CosmeticsVoluntary Action Indicated (VAI)2016539
Jan 26, 2012City Of Industry, CAFood/CosmeticsNo Action Indicated (NAI)2016539
Aug 30, 2010City Of Industry, CAFood/CosmeticsVoluntary Action Indicated (VAI)2016539
Sep 23, 2009City Of Industry, CAFood/CosmeticsVoluntary Action Indicated (VAI)2016539

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 2016539City Of Industry, CA8Jan 27, 2026

FDA data resources

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