FDA inspection

Howmedica Osteonics Corp. d.b.a. Stryker Spine: FDA inspection ending Aug 26, 2009

FDA inspection 607268 · Voluntary Action Indicated (VAI) · Summit, NJ

Key facts

Inspection ID 607268
Firm Howmedica Osteonics Corp. d.b.a. Stryker Spine
FEI number 3003890623
Address 475 Springfield Ave Fl 4
City Summit
State NJ
ZIP 07901
Country United States
Fiscal year 2009
Inspection end date Aug 26, 2009
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
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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