FDA inspection

MEDINVENTS NV: FDA inspection ending Jan 24, 2013

FDA inspection 820733 · Voluntary Action Indicated (VAI) · Hasselt

Key facts

Inspection ID 820733
Firm MEDINVENTS NV
FEI number 3007513241
Address Kuringersteenweg 304
City Hasselt
Country Belgium
Fiscal year 2013
Inspection end date Jan 24, 2013
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices
Warning letter 396903

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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