FDA inspection

LivaNova Deutschland GmbH: FDA inspection ending Sep 23, 2005

FDA inspection 409997 · No Action Indicated (NAI) · Munich

Key facts

Inspection ID 409997
Firm LivaNova Deutschland GmbH
FEI number 3002808267
Address Lindberghstr. 25
City Munich
Fiscal year 2005
Inspection end date Sep 23, 2005
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
  • 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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