FDA inspection

Cortex Technology ApS: FDA inspection ending Jun 9, 2015

FDA inspection 929307 · No Action Indicated (NAI) · Aalborg Ost

Key facts

Inspection ID 929307
Firm Cortex Technology ApS
FEI number 3002987034
Address Plastvanget 9
City Aalborg Ost
Country Denmark
Fiscal year 2015
Inspection end date Jun 9, 2015
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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