# Visura Technologies, Inc. – FDA 483, Mar 24, 2026

Source: https://www.keypedia.com/records/483/visura-technologies-inc/decc7d2d-dfd0-4303-a1c3-938d0a2b8983

> FDA 483 for Visura Technologies, Inc. on March 24, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Visura Technologies, Inc.
- Inspection Date: 2026-03-24
- Product Type: device
- Office Name: Minneapolis District Office
- Summary: Visura Technologies, Inc. in Minneapolis was inspected by the FDA from March 22-24, 2026. The inspection revealed that the firm failed to adequately document procedures for timely complaint handling. Specifically, five cases alleging malfunction of their transesophageal echocardiogram (TEE) camera assist device were not identified and documented as complaints, leading to potential patient safety concerns.

## Related Officers

- [Albert L. Nguyen](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