FDA Inspection 1108789 - Medtronic Neuromodulation - October 17, 2019

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Record Details

This FDA Inspection record concerns Medtronic Neuromodulation, with an inspection on October 17, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic Neuromodulation
Inspection Date: October 17, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 08b518e7-00db-4f3d-8411-5c55da4a26c8

Violation Codes2

21 CFR 820.100(a)21 CFR 820.30(c)

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