FDA-Inspected Site

MediStim ASA

2 FDA inspections are on record for MediStim ASA in Horten, Norway.

483· Form 483 issued

Horten, Norway · Last updated July 9, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2017-08-25.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
25 Aug 2017Medical Devices & Rad Health483View 483 →
22 Apr 2004Not recordedClean

Observations on record

Form 483 observations cited at this site, most recent first.

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

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

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 site report

Get the verbatim findings behind MediStim ASA's 1 Form 483

Recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat