FDA inspection

Stryker Corporation: FDA inspection ending Nov 9, 2012

FDA inspection 806763 · Official Action Indicated (OAI) · Portage, MI

Key facts

Inspection ID 806763
Firm Stryker Corporation
FEI number 1811755
Address 4100 E Milham Ave
City Portage
State MI
ZIP 49002
Country United States
Fiscal year 2013
Inspection end date Nov 9, 2012
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices
Warning letter 388982

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes 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

Browse all FDA inspections