Form 483

Barco N.V. Form 483, 2023-09-14

FDA issued a Form 483 to Barco N.V. on 2023-09-14 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Barco N.V. · Kortrijk, Belgium · Issued September 14, 2023

Overview

  • 6 public-safe observations are available for this inspection.
  • 6 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.

14 Sep 2023
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Esteban Beltran

14 Sep 2023
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Esteban Beltran

14 Sep 2023
21 CFR 820.198(c)

Investigation of device failures

Cited by Esteban Beltran

14 Sep 2023
21 CFR 820.198(d)

Evaluation, timeliness, identification

Cited by Esteban Beltran

14 Sep 2023
21 CFR 820.25(b)

Training records

Cited by Esteban Beltran

Inspected site

BNBarco N.V.Kortrijk, Belgium

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17Cited across public-safe Form 483 observations1x
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.198(c)Cited across public-safe Form 483 observations1x
21 CFR 820.198(d)Cited across public-safe Form 483 observations1x
21 CFR 820.25(b)Cited across public-safe Form 483 observations1x
21 CFR 820.50Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 6 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