FDA Inspection 1206222 - Medtronic Neuromodulation - May 05, 2023

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Record Details

This FDA Inspection record concerns Medtronic Neuromodulation, with an inspection on May 5, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic Neuromodulation
Inspection Date: May 5, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ca41952b-debf-4e58-9a3d-a67b671f3055

Violation Codes4

21 CFR 803.17(a)(1)21 CFR 806.10(b)21 CFR 820.100(a)21 CFR 820.198(c)

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