FDA Inspection
Nevro CorporationNevro Corporation – FDA Inspection, May 2, 2013
Record Details
This FDA Inspection record concerns Nevro Corporation, with an inspection on May 2, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Nevro Corporation
- Inspection Date
- May 2, 2013
- Product Type
- Devices
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ID · bbff2711-ab1c-45d8-9075-27985acc570d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 832134
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.7(a)Promotion or test marketing
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Nevro Corporation
9| Date | Classification | Office | Project area |
|---|---|---|---|
| August 13, 2025 | OAI | San Francisco District Office | Postmarket Assurance: Medical Devices |
| December 20, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 26, 2022 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 21, 2019 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 16, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Nevro Corporation
- FDA Inspection 1276522 - 2025-08-13
- FDA Inspection 1226345 - 2023-12-20
- FDA Inspection 1169416 - 2022-04-26
- FDA Inspection 1088855 - 2019-03-21
- FDA Inspection 1046576 - 2018-03-16
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