# FDA Inspection 982335 - Nevro Corporation - August 26, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/nevro-corporation/fbf655b9-857c-4367-bd7c-daa9638322e1/
Source feed: FDA_Inspections

> FDA Inspection 982335 for Nevro Corporation on August 26, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 982335
- Company Name: Nevro Corporation
- Inspection Date: 2016-08-26
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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