Reliance Private Label Supplements

FDA Regulatory Profile

Reliance Private Label Supplements has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 16, 2025 · 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
Inspections6Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 16, 2025Edison, NJFood/CosmeticsNo Action Indicated (NAI)2245259
Jun 29, 2018Edison, NJFood/CosmeticsNo Action Indicated (NAI)2245259
Sep 28, 2015Edison, NJFood/CosmeticsNo Action Indicated (NAI)2245259
Sep 28, 2015Edison, NJFood/CosmeticsNo Action Indicated (NAI)2245259
Aug 3, 2010Edison, NJFood/CosmeticsVoluntary Action Indicated (VAI)2245259
Apr 20, 2009Edison, NJFood/CosmeticsNo Action Indicated (NAI)2245259

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 2245259Edison, NJ6Sep 16, 2025

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