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FDA Inspection 982335 — Nevro Corporation

Nevro Corporation — FEI 3008514029

The FDA completed an inspection of Nevro Corporation on August 26, 2016 in Redwood City, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 26, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Redwood City, CA (United States)

Additional Details

Postmarket Audit Inspections

Facility

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