FDA inspection

Stryker Craniomaxillofacial Division: FDA inspection ending Oct 4, 2006

FDA inspection 446983 · Portage, MI

Key facts

Inspection ID 446983
Firm Stryker Craniomaxillofacial Division
FEI number 3005101424
Address 750 Trade Centre Way Ste 200
City Portage
State MI
ZIP 49002-0482
Fiscal year 2007
Inspection end date Oct 4, 2006
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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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