FDA Inspection 1259483 - KANEKA MEDIX CORPORATION KANAGAWA PLANT - January 30, 2025

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Record Details

This FDA Inspection record concerns KANEKA MEDIX CORPORATION KANAGAWA PLANT, with an inspection on January 30, 2025, issued by the Center for Devices and Radiological Health, covering devices.

Company: KANEKA MEDIX CORPORATION KANAGAWA PLANT
Inspection Date: January 30, 2025
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 099efb48-e1db-4eea-96b4-e8199d337e03

Violation Codes2

21 CFR 820.100(a)21 CFR 820.90(a)

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