FDA Inspection 1022524 - Medtronic Neuromodulation - June 07, 2017

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Record Details

This FDA Inspection record concerns Medtronic Neuromodulation, with an inspection on June 7, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic Neuromodulation
Inspection Date: June 7, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0aeb6773-82b6-44a3-897d-bc5c8242f9ba