Form 483

Cortex Technology ApS Form 483, 2018-06-13

FDA issued a Form 483 to Cortex Technology ApS on 2018-06-13 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Cortex Technology ApS · Aalborg Ost, Denmark · Issued June 13, 2018

Overview

  • 4 public-safe observations are available for this inspection.
  • 2 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

13 Jun 2018
21 CFR 820.30(c)

Design input - documentation

Cited by Lisa A Warner

13 Jun 2018
21 CFR 820.30(c)

Design input - documentation

Cited by Lisa A Warner

13 Jun 2018
21 CFR 820.30(g)

Design validation- Lack of or inadequate procedures

Cited by Lisa A Warner

13 Jun 2018
21 CFR 820.30(g)

Design validation- Lack of or inadequate procedures

Cited by Lisa A Warner

Inspected site

CTCortex Technology ApSAalborg Ost, Denmark

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.30(c)Cited across public-safe Form 483 observations2x
21 CFR 820.30(g)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 4 observations

The full inspection record, as Atlas holds it, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere