FDA Inspection 1187313 - Medtronic Neuromodulation - November 03, 2022

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Record Details

This FDA Inspection record concerns Medtronic Neuromodulation, with an inspection on November 3, 2022, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic Neuromodulation
Inspection Date: November 3, 2022
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0826f3ee-c543-4555-ad61-9cede8f200b3

Violation Codes2

21 CFR 806.10(a)(1)21 CFR 820.100(a)

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