S & S X-Ray Products, Inc.
S & S X-Ray Products, Inc. has 0 FDA recalls, 3 inspections, 4 510(k) clearances and 1 compliance action on record.
- Latest inspection
- Mar 9, 2020 · VAI
- Latest 510(k)
- Aug 4, 2003
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 4, 2026 (checked Nov 8, 2026, unchanged) | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 4 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 3 | Nov 10, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 1 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Mar 9, 2020 | Houston, TX | Devices | Voluntary Action Indicated (VAI) | 1650045 |
| Mar 28, 2019 | Houston, TX | Devices | No Action Indicated (NAI) | 1650045 |
| Mar 23, 2011 | Houston, TX | Devices | No Action Indicated (NAI) | 1650045 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 1650045 | Houston, TX | 3 | Mar 9, 2020 |