FDA inspection

Bricon Technology GmbH: FDA inspection ending Feb 27, 2014

FDA inspection 867227 · Voluntary Action Indicated (VAI) · Wurmlingen

Key facts

Inspection ID 867227
Firm Bricon Technology GmbH
FEI number 3004072627
Address Eisenbahnstr. 100
City Wurmlingen
Country Germany
Fiscal year 2014
Inspection end date Feb 27, 2014
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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