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Shenzhen Jamr Medical Technology Co., Ltd.

FDA Regulatory Profile

Shenzhen Jamr Medical Technology Co., Ltd. has 0 FDA recalls, 1 inspection, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Jun 5, 2019 · OAI
Latest 510(k)
Jun 30, 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
Inspections1Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 5, 2019Shenzhen, ChinaDevicesOfficial Action Indicated (OAI)3014166838

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
K220651Wrist Type Blood Pressure MonitorJun 30, 2022

FDA data resources