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Taejoon Pharmaceutical Co., Ltd.

FDA Regulatory Profile

Taejoon Pharmaceutical Co., Ltd. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Oct 18, 2022 · VAI

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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
Inspections3Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Oct 18, 2022Yongin, Korea (The Republic Of)DrugsVoluntary Action Indicated (VAI)3008029795
Oct 15, 2019Yongin, Korea (The Republic Of)DrugsOfficial Action Indicated (OAI)3008029795
Nov 15, 2016Yongin, Korea (The Republic Of)DrugsVoluntary Action Indicated (VAI)3008029795

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 3008029795Yongin, Korea (The Republic Of)3Oct 18, 2022

FDA data resources

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