FDA inspection

Ottobock SE & Co. KGaA Formerly Known As Otto Bock Healthcare GmbH: FDA inspection ending Nov 27, 2014

FDA inspection 909450 · No Action Indicated (NAI) · Duderstadt

Key facts

Inspection ID 909450
Firm Ottobock SE & Co. KGaA Formerly Known As Otto Bock Healthcare GmbH
FEI number 3003117657
Address Max-Nader-Str. # 15
City Duderstadt
Country Germany
Fiscal year 2015
Inspection end date Nov 27, 2014
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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