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

FDA Inspection 1211239 for CO-AX Technology Inc on August 02, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1211239 for CO-AX Technology Inc on August 02, 2023. Classification: Voluntary Action Indicated (VAI).

Violation Codes

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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Record Information

Company

CO-AX Technology Inc

Inspection Date

August 2, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

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

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