FDA inspection

Nevro Corporation: FDA inspection ending Nov 1, 2012

FDA inspection 804964 · Voluntary Action Indicated (VAI) · Redwood City, CA

Key facts

Inspection ID 804964
Firm Nevro Corporation
FEI number 3008514029
Address 1800 Bridge Pkwy
City Redwood City
State CA
ZIP 94065
Country United States
Fiscal year 2013
Inspection end date Nov 1, 2012
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

Browse all FDA inspections