# Nevro Corporation – FDA Inspection, Nov 3, 2017

Source: https://www.keypedia.com/records/fda_inspections/nevro-corporation/b553accd-8391-4b02-b454-100ea8d935a0
Source feed: FDA_Inspections

> FDA inspection 1030660 of Nevro Corporation, November 03, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued. 9 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030660
- Company Name: Nevro Corporation
- Inspection Date: 2017-11-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/adam-s-freeman/8bbc5e50-32c6-4559-b5c9-01b88d102450)

Company: https://www.keypedia.com/companies/nevro-corporation/6d7059fd-516e-436a-a674-209ff30a5b2c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7