FDA Inspection 1059011 - Medtronic Neuromodulation - June 21, 2018

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Record Details

This FDA Inspection record concerns Medtronic Neuromodulation, with an inspection on June 21, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic Neuromodulation
Inspection Date: June 21, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ee76f5e3-419c-4ba2-9589-3dc503f70956