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Hubei Qianjiang Kingphar Medical Material Co., Ltd.

FDA Regulatory Profile

Hubei Qianjiang Kingphar Medical Material Co., Ltd. has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Jul 3, 2025 · OAI
Latest 510(k)
Jul 19, 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) clearances1Oct 4, 2026Not statedCurrent
Inspections2Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 3, 2025Qian Jiang, ChinaDevicesOfficial Action Indicated (OAI)3002897187
Apr 25, 2013Qian Jiang, ChinaDevicesVoluntary Action Indicated (VAI)3002897187

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
K220777Surgical face maskJul 19, 2022

FDA data resources