FDA inspection

Nevro Corporation: FDA inspection ending Mar 16, 2018

FDA inspection 1046576 · No Action Indicated (NAI) · Redwood City, CA

Key facts

Inspection ID 1046576
Firm Nevro Corporation
FEI number 3008514029
Address 1800 Bridge Pkwy
City Redwood City
State CA
ZIP 94065
Country United States
Fiscal year 2018
Inspection end date Mar 16, 2018
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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

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