Form 483

Orfit Industries NV Form 483, 2018-05-17

FDA issued a Form 483 to Orfit Industries NV on 2018-05-17 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Orfit Industries NV · Wijnegem, Belgium · Issued May 17, 2018

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 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.

17 May 2018
21 CFR 820.20(c)

Management review - defined interval, sufficient frequency

Cited by Yehualashet A Gessesse

17 May 2018
21 CFR 820.22

Quality Audits - defined intervals

Cited by Yehualashet A Gessesse

17 May 2018
21 CFR 820.30(e)

Design review - documentation

Cited by Yehualashet A Gessesse

Inspected site

OIOrfit Industries NVWijnegem, Belgium

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.20(c)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.30(e)Cited across public-safe Form 483 observations1x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 3 observations

The source PDF and every observation in full, 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