FDA Inspection 1030660 - Nevro Corporation - November 03, 2017

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Record Details

This FDA Inspection record concerns Nevro Corporation, with an inspection on November 3, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Nevro Corporation
Inspection Date: November 3, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 48d96f92-4700-4120-b8ef-b7ae90aa934a

Violation Codes5

21 CFR 803.50(a)(1)21 CFR 820.100(a)21 CFR 820.198(c)21 CFR 820.30(g)21 CFR 820.75(a)

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