FDA inspection

Karl Storz SE & Co. KG: FDA inspection ending Oct 18, 2012

FDA inspection 807643 · Voluntary Action Indicated (VAI) · Tuttlingen

Key facts

Inspection ID 807643
Firm Karl Storz SE & Co. KG
FEI number 3002808268
Address Mittelstrasse 8
City Tuttlingen
Country Germany
Fiscal year 2013
Inspection end date Oct 18, 2012
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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