FDA Inspection 993878 - Aionex, Inc. - December 02, 2016

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Record Details

This FDA Inspection record concerns Aionex, Inc., with an inspection on December 2, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Aionex, Inc.
Inspection Date: December 2, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 20e2fb2b-fdc4-4d2d-b956-c23d1dc186cc