Shenzhen Pacom Medical Instruments Co., Ltd.

FDA Regulatory Profile

Shenzhen Pacom Medical Instruments Co., Ltd. has 0 FDA recalls, 1 inspection, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 30, 2024 · NAI
Latest 510(k)
Dec 13, 2019

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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 23, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
May 30, 2024Shenzhen, ChinaDevicesNo Action Indicated (NAI)3013147512

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
K190717Infrared Thermometer, model: PC808Dec 13, 2019
K172889Infrared ThermometerMay 25, 2018