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GEV Co.,Ltd.

FDA Regulatory Profile

GEV Co.,Ltd. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 17, 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
Inspections4Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 17, 2025Eumseong, Korea (The Republic Of)BiologicsNo Action Indicated (NAI)3010501626
Sep 6, 2023Eumseong, Korea (The Republic Of)BiologicsVoluntary Action Indicated (VAI)3010501626
Apr 16, 2019Eumseong, Korea (The Republic Of)BiologicsNo Action Indicated (NAI)3010501626
May 27, 2014Eumseong, Korea (The Republic Of)BiologicsNo Action Indicated (NAI)3010501626

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 3010501626Eumseong, Korea (The Republic Of)4Sep 17, 2025

FDA data resources

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