FDA Inspection
USHIO GERMANY GmbHFDA 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.
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ID · 53c6ade7-b7a8-48f4-b50c-f981f73b546b
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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