FDA inspection

Cortex Technology ApS: FDA inspection ending Oct 31, 2011

FDA inspection 751599 · Voluntary Action Indicated (VAI) · Aalborg Ost

Key facts

Inspection ID 751599
Firm Cortex Technology ApS
FEI number 3002987034
Address Plastvanget 9
City Aalborg Ost
Country Denmark
Fiscal year 2012
Inspection end date Oct 31, 2011
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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