FDA inspection

Eizo GmbH: FDA inspection ending Aug 22, 2014

FDA inspection 895411 · Voluntary Action Indicated (VAI) · Rulzheim

Key facts

Inspection ID 895411
Firm Eizo GmbH
FEI number 3006615345
Address Carl-Benz-Str. 3
City Rulzheim
Country Germany
Fiscal year 2014
Inspection end date Aug 22, 2014
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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