FDA inspection

Stryker Medical Division of Stryker Corporation: FDA inspection ending Jun 26, 2012

FDA inspection 791490 · Voluntary Action Indicated (VAI) · Portage, MI

Key facts

Inspection ID 791490
Firm Stryker Medical Division of Stryker Corporation
FEI number 1831750
Address 3800 E Centre Ave
City Portage
State MI
ZIP 49002
Country United States
Fiscal year 2012
Inspection end date Jun 26, 2012
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
  • 10–99 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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