FDA Inspection 1058782 - DuoProSS Meditech Corporation - July 13, 2018

Record Details

This FDA Inspection record concerns DuoProSS Meditech Corporation, with an inspection on July 13, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: DuoProSS Meditech Corporation
Inspection Date: July 13, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · da92356f-2b64-4125-9700-ed9c4fa732fb

Violation Codes3

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)

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