FDA inspection

Stryker Spine: FDA inspection ending Feb 10, 2016

FDA inspection 966647 · No Action Indicated (NAI) · Cestas, Nouvelle-Aquitaine

Key facts

Inspection ID 966647
Firm Stryker Spine
FEI number 3003112432
Address Zone Industrielle De Marticot
City Cestas, Nouvelle-Aquitaine
Country France
Fiscal year 2016
Inspection end date Feb 10, 2016
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
  • 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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