FDA Inspection 1195261 - AxioMed, LLC. - January 13, 2023

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Record Details

This FDA Inspection record concerns AxioMed, LLC., with an inspection on January 13, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: AxioMed, LLC.
Inspection Date: January 13, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1d0e2d9f-ba64-4c4f-a0fa-5c58316a436e

Violation Codes1

21 CFR 812.150(b)(5)

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