FDA-Inspected Site

Visura Technologies, Inc.

2 FDA inspections are on record for Visura Technologies, Inc. in Minneapolis, United States.

483· Form 483 issued

Minneapolis, United States · Last updated August 15, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2026-03-24.

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
23 Mar 2026 – 24 Mar 2026Medical Devices & Rad Health483View 483 →
5 Nov 2019Medical Devices & Rad HealthClean

Observations on record

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

24 Mar 2026
ISO 13485:2016 Clause 8.2.2

Complaint handling procedures not documented

Cited by Albert L Nguyen

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
ISO 13485:2016 Clause 8.2.2Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Visura Technologies, Inc.'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