FDA Inspection 955935 - Riken Keiki Co., Ltd. - December 09, 2015

Record Details

This FDA Inspection record concerns Riken Keiki Co., Ltd., with an inspection on December 9, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Riken Keiki Co., Ltd.
Inspection Date: December 9, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4534df36-3ac7-434d-8a63-0946e8944008

Violation Codes3

21 CFR 803.1721 CFR 803.18(a)21 CFR 820.30(g)

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