WISETRADE CORPORATION
FDA Regulatory Profile
WISETRADE CORPORATION has 1 FDA recall (1 Class I), 2 inspections, 0 510(k) clearances and 1 compliance action on record.
- Latest recall
- F-1009-2022 · Class I · Mar 23, 2022
- Latest inspection
- Dec 6, 2023 · NAI
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Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 1 (1 Class I) | Nov 4, 2026 (checked Nov 8, 2026, unchanged) | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 2 | Nov 9, 2026 | Newest record Oct 28, 2026 | Current |
|---|
| Compliance actions | 1 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent Recalls
| Number | Class | Product | Date |
|---|
| F-1009-2022 | Class I | Global Fresh Marketing Enoki Mushrooms Champignons d'Enoki Net Wt/Poids 200g/7.05 oz. Vacuumed… | Mar 23, 2022 |
Recent FDA Inspections
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 3020706490 | Irvine, CA | 2 | Dec 6, 2023 |