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SCI Pharmtech Inc.

FDA Regulatory Profile

SCI Pharmtech Inc. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 6, 2025 · VAI

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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
Inspections5Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 6, 2025Taoyuan City, TaiwanDrugsVoluntary Action Indicated (VAI)3004065859
Sep 5, 2019Taoyuan City, TaiwanDrugsNo Action Indicated (NAI)3004065859
Sep 15, 2017Taoyuan City, TaiwanDrugsVoluntary Action Indicated (VAI)3004065859
Dec 19, 2014Taoyuan City, TaiwanDrugsNo Action Indicated (NAI)3004065859
Apr 20, 2012Taoyuan City, TaiwanDrugsVoluntary Action Indicated (VAI)3004065859

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 3004065859Taoyuan City, Taiwan5Jun 6, 2025

FDA data resources

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