MediView XR Minnesota Office FDA Record
- Latest inspection NAI · Jul 10, 2025
- No warning letters matched by name
MediView XR Minnesota Office has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "MediView XR Minnesota Office" is on file.
- Latest inspection
- Jul 10, 2025 · NAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 1 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Jul 10, 2025 | Roseville, MN | Devices | No Action Indicated (NAI) | 3030598507 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3030598507 | Roseville, MN | 1 | Jul 10, 2025 |
MediView XR Minnesota Office and the FDA: common questions
Has MediView XR Minnesota Office received an FDA warning letter?
No FDA warning letter addressed to the name "MediView XR Minnesota Office" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has MediView XR Minnesota Office received an FDA Form 483?
FDA has not published a Form 483 for "MediView XR Minnesota Office" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect MediView XR Minnesota Office?
The most recent FDA inspection on file ended Jul 10, 2025 at Roseville, MN and was classified NAI. FDA has 1 inspection of MediView XR Minnesota Office on file.
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