Koryeo International Corp.

FDA Regulatory Profile

Koryeo International Corp. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Aug 12, 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
Inspections5Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 12, 2025Jersey City, NJFood/CosmeticsNo Action Indicated (NAI)2434021
Mar 23, 2018Jersey City, NJFood/CosmeticsNo Action Indicated (NAI)2434021
Mar 20, 2015Jersey City, NJFood/CosmeticsNo Action Indicated (NAI)2434021
Aug 6, 2014Jersey City, NJFood/CosmeticsOfficial Action Indicated (OAI)2434021
Feb 17, 2012Jersey City, NJFood/CosmeticsVoluntary Action Indicated (VAI)2434021

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 2434021Jersey City, NJ5Aug 12, 2025

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