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FDA Inspection
•DuoProSS Meditech Corporation•August 12, 2022

FDA Inspection 1177699 - DuoProSS Meditech Corporation - August 12, 2022

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Record Details

This FDA Inspection record concerns DuoProSS Meditech Corporation, with an inspection on August 12, 2022, issued by the Center for Devices and Radiological Health, covering devices.

Company
DuoProSS Meditech Corporation
Inspection Date
August 12, 2022
Product Type
Devices
Office
Center for Devices and Radiological Health
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ID · 017bad51-0ab7-400c-8fdc-d4a2678675eb

Violation Codes3
21 CFR 803.1721 CFR 820.100(a)21 CFR 820.80(a)

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