FDA Inspection 999605 - Hebei Pukang Medical Instruments Co., Ltd. - January 12, 2017

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Record Details

This FDA Inspection record concerns Hebei Pukang Medical Instruments Co., Ltd., with an inspection on January 12, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Hebei Pukang Medical Instruments Co., Ltd.
Inspection Date: January 12, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0b144080-4367-4157-bb1e-1a257f0bb34b

Violation Codes8

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.18421 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.30(a)21 CFR 820.75(a)

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FDA Inspection

Hebei Pukang Medical Instruments Co., Ltd.January 12, 2017