FDA Inspection 1276522 - Nevro Corporation - August 13, 2025

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Record Details

This FDA Inspection record concerns Nevro Corporation, with an inspection on August 13, 2025, issued by the Center for Devices and Radiological Health, covering devices.

Company: Nevro Corporation
Inspection Date: August 13, 2025
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 9eef171f-4f70-4a3e-889a-eef42a415d86

Violation Codes6

21 CFR 803.50(a)(1)21 CFR 820.100(b)21 CFR 820.198(a)21 CFR 820.30(g)21 CFR 820.70(a)21 CFR 820.75(a)

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