FDA inspection

Nuvasive Inc: FDA inspection ending Oct 26, 2016

FDA inspection 991304 · Voluntary Action Indicated (VAI) · Fairborn, OH

Key facts

Inspection ID 991304
Firm Nuvasive Inc
FEI number 3009885359
Address 1 Herald Sq
City Fairborn
State OH
ZIP 45324
Country United States
Fiscal year 2017
Inspection end date Oct 26, 2016
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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
  • 1–9 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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