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Orient Pharma Co., Ltd.

FDA Regulatory Profile

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

Latest inspection
May 23, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections4Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 23, 2025Yunlin County, TaiwanDrugsNo Action Indicated (NAI)3009057557
Nov 16, 2018Yunlin County, TaiwanDrugsNo Action Indicated (NAI)3009057557
Apr 3, 2015Yunlin County, TaiwanDrugsVoluntary Action Indicated (VAI)3009057557
Dec 14, 2012Yunlin County, TaiwanDrugsNo Action Indicated (NAI)3009057557

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 3009057557Yunlin County, Taiwan4May 23, 2025

FDA data resources

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