Form 483

MediStim ASA Form 483, 2017-08-25

FDA issued a Form 483 to MediStim ASA on 2017-08-25 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

MediStim ASA · Horten, Norway · Issued August 25, 2017

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.

25 Aug 2017
21 CFR 820.184

DHR content

Cited by Adam S Freeman

25 Aug 2017
21 CFR 820.50(a)

Evaluation of suppliers, contractors, etc., requirements

Cited by Adam S Freeman

25 Aug 2017
21 CFR 820.75(a)

Documentation

Cited by Adam S Freeman

Inspected site

MAMediStim ASAHorten, Norway

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.50(a)Cited across public-safe Form 483 observations1x
21 CFR 820.75(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