FDA inspection

Stryker Spine: FDA inspection ending Jun 8, 2005

FDA inspection 385837 · Official Action Indicated (OAI) · Cestas, Aquitane

Key facts

Inspection ID 385837
Firm Stryker Spine
FEI number 3003112432
Address Zone Industrielle De Marticot
City Cestas, Aquitane
Fiscal year 2005
Inspection end date Jun 8, 2005
Classification Official Action Indicated (OAI)
Project area Product Evaluation: Med 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

Browse all FDA inspections