# Visura Technologies, Inc. – FDA Inspection, Mar 24, 2026

Source: https://www.keypedia.com/records/fda_inspections/visura-technologies-inc/93107a73-a241-4d08-a4a4-0b96a579d112
Source feed: FDA_Inspections

> FDA inspection 1300774 of Visura Technologies, Inc., March 24, 2026. Classification: Voluntary Action Indicated (VAI). 1 citation. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1300774
- Company Name: Visura Technologies, Inc.
- Inspection Date: 2026-03-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Minneapolis District Office
- Citation Count: 1

## Related Documents

- FDA Inspection 1111021 - 2019-11-05

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/albert-l-nguyen/496338d0-71c4-43da-92f0-09515559d9fc)

Company: https://www.keypedia.com/companies/visura-technologies-inc/25211dd8-7475-41f6-a998-99ac9dceddd5

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d