FDA Inspection 1211239 - CO-AX Technology Inc - August 02, 2023

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Record Details

This FDA Inspection record concerns CO-AX Technology Inc, with an inspection on August 2, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: CO-AX Technology Inc
Inspection Date: August 2, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · fe5fbed3-0a0e-450f-ba43-bf7ee9825cd6

Violation Codes9

21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.50(a)(2)21 CFR 820.50(b)21 CFR 820.72(a)21 CFR 820.75(a)21 CFR 820.80(b)21 CFR 820.90(a)21 CFR 820.90(b)(2)

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