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 medical devices & rad health.

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

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ID · a781100d-8356-48d5-a2eb-58b3416a82d9

Violation Codes2

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

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