FDA Inspection 1095111 - Neurolign USA, Llc - July 02, 2019

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Record Details

This FDA Inspection record concerns Neurolign USA, Llc, with an inspection on July 2, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Neurolign USA, Llc
Inspection Date: July 2, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 3c519d48-fd7b-4b35-ae53-92c97469ec95