FDA inspection

Eurotrol B.V.: FDA inspection ending May 22, 2014

FDA inspection 883233 · Official Action Indicated (OAI) · Ede Gld

Key facts

Inspection ID 883233
Firm Eurotrol B.V.
FEI number 3005695774
Address Keplerlaan 20
City Ede Gld
Country Netherlands
Fiscal year 2014
Inspection end date May 22, 2014
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices
Warning letter 433999

At a glance

  • None Citations
  • 1–9 Posted citations
  • Yes 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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