FDA Inspection 1016443 - Medtronic Neuromodulation - June 30, 2017

Record Details

This FDA Inspection record concerns Medtronic Neuromodulation, with an inspection on June 30, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic Neuromodulation
Inspection Date: June 30, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · dc924c14-2eef-491d-a294-73fc7826b1b6

Violation Codes2

21 CFR 820.100(a)21 CFR 820.198(c)

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