FDA Inspection 1102180 - Medtronic Neuromodulation - August 06, 2019

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Record Details

This FDA Inspection record concerns Medtronic Neuromodulation, with an inspection on August 6, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic Neuromodulation
Inspection Date: August 6, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ffaaee90-31c0-4a0a-8024-c623571f25d7