FDA Inspection 1019051 - HUREV Co., Ltd. - June 29, 2017

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Record Details

This FDA Inspection record concerns HUREV Co., Ltd., with an inspection on June 29, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: HUREV Co., Ltd.
Inspection Date: June 29, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · f6dc6bc0-5567-44f4-a535-1ba90865fd2f

Violation Codes7

21 CFR 820.100(a)21 CFR 820.18421 CFR 820.70(c)21 CFR 820.70(f)21 CFR 820.70(g)21 CFR 820.75(b)21 CFR 820.80(d)

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