FDA inspection

KARL STORZ GMBH & CO. KG: FDA inspection ending Mar 4, 2016

FDA inspection 976641 · Voluntary Action Indicated (VAI) · Tuttlingen

Key facts

Inspection ID 976641
Firm KARL STORZ GMBH & CO. KG
FEI number 3006546082
Address Elsa-Brandstrom-Weg 21
City Tuttlingen
Fiscal year 2016
Inspection end date Mar 4, 2016
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None 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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