FDA Inspection 1056265 - Biomedix Wai - June 08, 2018

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Record Details

This FDA Inspection record concerns Biomedix Wai, with an inspection on June 8, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Biomedix Wai
Inspection Date: June 8, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 39e96508-58cd-4e5f-b152-ba8dc19d54c5

Violation Codes10

21 CFR 803.1721 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.250(b)21 CFR 820.30(g)21 CFR 820.5021 CFR 820.70(a)21 CFR 820.70(c)

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