FDA Inspection 1016443 - Medtronic Neuromodulation - June 30, 2017

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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 · 035c2472-eaf2-4f42-b282-8bf64cb0b4f6

Violation Codes2

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

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