Famidoc Technology Co., Ltd.

FDA Regulatory Profile

Famidoc Technology Co., Ltd. has 0 FDA recalls, 1 inspection, 9 510(k) clearances and 0 compliance actions on record.

Latest inspection
Nov 5, 2015 · VAI
Latest 510(k)
Apr 5, 2024

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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) clearances9Oct 4, 2026Not statedCurrent
Inspections1Oct 23, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 5, 2015Dongguan, ChinaDevicesVoluntary Action Indicated (VAI)3005621440

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
K233192Wireless Smart ThermometerApr 5, 2024
K222887Arm Blood Pressure Monitor/Automatic Wireless Smart Blood Pressure MonitorApr 10, 2023
K212918Heat StimPlusDec 13, 2021
K191673Upper Arm Blood Pressure MonitorNov 27, 2019
K130723FDES106 MINI TENS&EMS DEVICE,FDES106 MULTI-FUNCTION MINI TENS&EMS DEVICE,FDES105 PAIN RELIEF…Feb 7, 2014
K113010FDES100(TENS AND EMS STIMULATOR, FDES102(ED402) TENS STIMULATORDec 21, 2012
K113761INFRARED THERMOMETERSep 7, 2012
K072641DIGITAL ELECTRONIC THERMOMETER, MODEL: FDTH-V0-1 THRU 4.Nov 1, 2007
K052849INFRARED THERMOMETER, FDIR-V1Oct 26, 2005