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

Source: https://www.keypedia.com/records/fda_inspections/nevro-corporation/14f3a56f-c084-4e20-9dba-1b13940cc426
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276522
- Company Name: Nevro Corporation
- Inspection Date: 2025-08-13
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: San Francisco District Office

## Related Documents

- [FDA Inspection 1276522 - 2025-08-13](https://www.keypedia.com/records/fda_inspections/nevro-corporation/93e5dd0a-95b1-424d-bdb6-527d93f07114)
- [FDA Inspection 1276522 - 2025-08-13](https://www.keypedia.com/records/fda_inspections/nevro-corporation/129fa569-f52f-44c3-b030-7a974f75bdd4)
- [FDA Inspection 1276522 - 2025-08-13](https://www.keypedia.com/records/fda_inspections/nevro-corporation/9eef171f-4f70-4a3e-889a-eef42a415d86)
- [FDA Inspection 1226345 - 2023-12-20](https://www.keypedia.com/records/fda_inspections/nevro-corporation/1cdca5de-fcf4-4535-9e93-18d11291b73c)
- [FDA Inspection 1226345 - 2023-12-20](https://www.keypedia.com/records/fda_inspections/nevro-corporation/8e6d8185-5da9-474a-8b3d-f9f062f358ff)

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

Office: https://www.keypedia.com/offices/san-francisco-district-office/6f838e9c-aae1-4665-9c46-a51d43be02df