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LCC Ltd.

FDA Regulatory Profile

LCC Ltd. has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 2 compliance actions on record.

Latest inspection
Mar 22, 2024 · OAI

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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
Inspections2Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 22, 2024Eumseong, Korea (The Republic Of)DrugsOfficial Action Indicated (OAI)3007255059
Dec 15, 2017Eumseong, Korea (The Republic Of)DrugsVoluntary Action Indicated (VAI)3007255059

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 3007255059Eumseong, Korea (The Republic Of)2Mar 22, 2024

FDA data resources

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