FDA inspection

Otto Bock Healthcare Products GmbH: FDA inspection ending Oct 17, 2012

FDA inspection 807571 · Voluntary Action Indicated (VAI) · Vienna

Key facts

Inspection ID 807571
Firm Otto Bock Healthcare Products GmbH
FEI number 3005190268
Address Brehmstrase 16
City Vienna
Country Austria
Fiscal year 2013
Inspection end date Oct 17, 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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