FDA inspection

Stryker Leibinger GmbH & Co. KG: FDA inspection ending Dec 16, 1999

FDA inspection 10349 · No Action Indicated (NAI) · Freiburg Im Breisgau

Key facts

Inspection ID 10349
Firm Stryker Leibinger GmbH & Co. KG
FEI number 3002821504
Address Botzinger Str. 41
City Freiburg Im Breisgau
Fiscal year 2000
Inspection end date Dec 16, 1999
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
  • 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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