# FDA Inspection 1276522 - Nevro Corporation - August 13, 2025

Source: https://www.keypedia.com/records/fda_inspections/nevro-corporation/9eef171f-4f70-4a3e-889a-eef42a415d86
Source feed: FDA_Inspections

> FDA Inspection 1276522 for Nevro Corporation on August 13, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276522
- Company Name: Nevro Corporation
- Inspection Date: 2025-08-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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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