JO Cosmetics Co., Ltd.

FDA Regulatory Profile

JO Cosmetics Co., Ltd. has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 22, 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
Inspections7Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 22, 2025Hanyu, JapanDrugsVoluntary Action Indicated (VAI)3006477904
Oct 26, 2018Ota, JapanDrugsVoluntary Action Indicated (VAI)3002695407
Oct 24, 2018Hanyu, JapanDrugsVoluntary Action Indicated (VAI)3006477904
Jul 14, 2017Ota, JapanDrugsVoluntary Action Indicated (VAI)3010164229
Jun 12, 2015Hanyu, JapanDrugsVoluntary Action Indicated (VAI)3006477904
Oct 3, 2013Ota, JapanDrugsVoluntary Action Indicated (VAI)3002695407
Oct 3, 2013Hanyu, JapanDrugsVoluntary Action Indicated (VAI)3006477904

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 3006477904Hanyu, Japan4May 22, 2025
FEI 3002695407Ota, Japan2Oct 26, 2018
FEI 3010164229Ota, Japan1Jul 14, 2017

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