FDA Inspection 969394 - The Metrix Company - May 06, 2016

Record Details

This FDA Inspection record concerns The Metrix Company, with an inspection on May 6, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: The Metrix Company
Inspection Date: May 6, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a06abbdd-4658-4578-838e-6df1add924c7

Violation Codes8

21 CFR 803.50(a)(2)21 CFR 806.10(a)(1)21 CFR 820.100(a)21 CFR 820.200(b)21 CFR 820.30(e)21 CFR 820.30(g)21 CFR 820.70(e)21 CFR 820.75(a)

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