FDA Inspection 1025529 - Huestis Machine Corporation - September 15, 2017

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Record Details

This FDA Inspection record concerns Huestis Machine Corporation, with an inspection on September 15, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Huestis Machine Corporation
Inspection Date: September 15, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1aaaf194-c856-4534-8f56-9ba9e0fa625c

Violation Codes10

21 CFR 1010.2(c)21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.30(g)21 CFR 820.30(i)21 CFR 820.5021 CFR 820.70(i)21 CFR 820.75(a)21 CFR 820.80(a)

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