Shenzhen Brav Electronic Technologies Co., Ltd.

FDA Regulatory Profile

Shenzhen Brav Electronic Technologies Co., Ltd. has 0 FDA recalls, 1 inspection, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Oct 13, 2023 · VAI
Latest 510(k)
Jul 17, 2023

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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
Inspections1Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Oct 13, 2023Shenzhen, ChinaDevicesVoluntary Action Indicated (VAI)3008975047

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
K211143Pulse OximeterJul 17, 2023
K171214Infrared ThermometerMar 2, 2018