FDA Inspection 1000208 - Lumitex Medical Devices Inc - January 09, 2017

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Record Details

This FDA Inspection record concerns Lumitex Medical Devices Inc, with an inspection on January 9, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Lumitex Medical Devices Inc
Inspection Date: January 9, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b6ad7ffd-a635-4358-9f4f-308397879d9b