FDA Inspection
Visura Technologies, Inc.Visura Technologies, Inc. – FDA Inspection, Mar 24, 2026
Record Details
This FDA Inspection record concerns Visura Technologies, Inc., with an inspection on March 24, 2026, issued by the Minneapolis District Office, covering medical devices & rad health.
- Company
- Visura Technologies, Inc.
- Inspection Date
- March 24, 2026
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 93107a73-a241-4d08-a4a4-0b96a579d112
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1300774
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Medical Devices
FDA Citations
1- ISO 13485:2016 Clause 8.2.2Complaint handling procedures not documented
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Visura Technologies, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 5, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Visura Technologies, Inc.
- FDA Inspection 1111021 - 2019-11-05
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