FDA inspection

Stryker Corporation: FDA inspection ending Aug 20, 2012

FDA inspection 793684 · No Action Indicated (NAI) · Portage, MI

Key facts

Inspection ID 793684
Firm Stryker Corporation
FEI number 3015967359
Address 3600 Holly Ln N Ste 40
City Portage
State MI
ZIP 49002
Country United States
Fiscal year 2012
Inspection end date Aug 20, 2012
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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