FDA Inspection 1259495 - Riken Keiki Co., Ltd. - January 30, 2025

Record Details

This FDA Inspection record concerns Riken Keiki Co., Ltd., with an inspection on January 30, 2025, issued by the Center for Devices and Radiological Health, covering devices.

Company: Riken Keiki Co., Ltd.
Inspection Date: January 30, 2025
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 992237d2-9a0e-4521-b8f0-2a51ef880839

Violation Codes8

21 CFR 803.1721 CFR 820.18421 CFR 820.20(b)(3)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.30(g)21 CFR 820.90(a)21 CFR 830.300(a)

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