Uscom Kft
FDA Regulatory Profile
Uscom Kft has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 1 compliance action on record.
- Latest inspection
- Mar 30, 2017 · VAI
Reviewing Uscom Kft as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Check this supplier
Or check Uscom Kft yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.
Get a free API key
Is this your company or a supplier you list? Link to this FDA record from your site with a free button.
Summary
Record counts and when each FDA source was last refreshed
| 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 11, 2026 | Newest record Nov 5, 2026 | Current |
|---|
| Compliance actions | 1 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Related names
| Name | Recalls | 510(k) | Inspections | Compliance | Most recent recall |
|---|
Uscom Limited
Same company group | 0 | 0 | 4 | 0 | — |
Uscom
Same company group | 0 | 1 | 0 | 0 | — |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|
| Mar 30, 2017 | Budapest, Hungary | Devices | Voluntary Action Indicated (VAI) | 3011382174 |
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|
| FEI 3011382174 | Budapest, Hungary | 1 | Mar 30, 2017 |