Form 483

Orfit Industries NV Form 483, 2022-11-10

FDA issued a Form 483 to Orfit Industries NV on 2022-11-10 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Orfit Industries NV · Wijnegem, Belgium · Issued November 10, 2022

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.

10 Nov 2022
21 CFR 820.22

Quality Audits - defined intervals

Cited by David J Gasparovich

10 Nov 2022
21 CFR 820.70(a)

Process control procedures, Lack of or inadequate procedures

Cited by David J Gasparovich

10 Nov 2022
21 CFR 820.90(a)

Nonconforming product, Lack of or inadequate procedures

Cited by David J Gasparovich

Inspected site

OIOrfit Industries NVWijnegem, Belgium

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.70(a)Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 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