FDA Inspection 952092 - Biomedix Wai - December 09, 2015

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Record Details

This FDA Inspection record concerns Biomedix Wai, with an inspection on December 9, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Biomedix Wai
Inspection Date: December 9, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 190b8c04-3652-4d38-b734-d59445edcdd2

Violation Codes7

21 CFR 820.100(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.30(g)21 CFR 820.5021 CFR 820.70(a)21 CFR 820.72(a)

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