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Wuxi Yushou Medical Appliances Co., Ltd.

FDA Regulatory Profile

Wuxi Yushou Medical Appliances Co., Ltd. has 0 FDA recalls, 2 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 28, 2017 · NAI
Latest 510(k)
Jan 18, 2022

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances2Oct 4, 2026Not statedCurrent
Inspections2Oct 27, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 28, 2017Wuxi, ChinaDevicesNo Action Indicated (NAI)3003829571
Jul 31, 2014Wuxi, ChinaDevicesNo Action Indicated (NAI)3003829571

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.

Recent 510(k) Clearances

K-NumberDeviceDate
K210679Medical Face MaskJan 18, 2022
K152906Disposable High Pressure Injector SyringeNov 22, 2016

FDA data resources