Quality Supplement Manufacturing, Inc.
Quality Supplement Manufacturing, Inc. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.
- Latest inspection
- Oct 18, 2023 · VAI
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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 | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 4 | Nov 9, 2026 | Newest record Oct 28, 2026 | Current |
| Compliance actions | 1 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Oct 18, 2023 | Oklahoma City, OK | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3011606714 |
| May 4, 2023 | Oklahoma City, OK | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3011606714 |
| Jun 13, 2022 | Oklahoma City, OK | Food/Cosmetics | Official Action Indicated (OAI) | 3011606714 |
| Mar 30, 2018 | Oklahoma City, OK | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3011606714 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3011606714 | Oklahoma City, OK | 4 | Oct 18, 2023 |