FDA Inspection 1100385 - USHIO GERMANY GmbH - August 23, 2019

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Record Details

This FDA Inspection record concerns USHIO GERMANY GmbH, with an inspection on August 23, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: USHIO GERMANY GmbH
Inspection Date: August 23, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b9da4ca1-c231-4d81-a2bb-6eee0d6712b1

Violation Codes6

21 CFR 820.100(a)21 CFR 820.18421 CFR 820.250(a)21 CFR 820.75(a)21 CFR 820.80(c)21 CFR 820.90(a)

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