FDA inspection

Stryker GmbH: FDA inspection ending Mar 27, 2025

FDA inspection 1263754 · Voluntary Action Indicated (VAI) · Selzach

Key facts

Inspection ID 1263754
Firm Stryker GmbH
FEI number 3002807830
Address Bohnackerweg 1
City Selzach
Country Switzerland
Fiscal year 2025
Inspection end date Mar 27, 2025
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
  • 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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