FDA inspection

Stryker Trauma GmbH: FDA inspection ending Nov 7, 2007

FDA inspection 498093 · No Action Indicated (NAI) · Schonkirchen

Key facts

Inspection ID 498093
Firm Stryker Trauma GmbH
FEI number 3002807231
Address Prof.-Kuntscher-Str. 1-5
City Schonkirchen
Fiscal year 2008
Inspection end date Nov 7, 2007
Classification No Action Indicated (NAI)
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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