FDA inspection

KARL STORZ GMBH & CO. KG: FDA inspection ending Oct 21, 2010

FDA inspection 698534 · No Action Indicated (NAI) · Tuttlingen

Key facts

Inspection ID 698534
Firm KARL STORZ GMBH & CO. KG
FEI number 3006546082
Address Elsa-Brandstrom-Weg 21
City Tuttlingen
Country Germany
Fiscal year 2011
Inspection end date Oct 21, 2010
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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