Multisource Manufacturing LLC
Multisource Manufacturing LLC has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Sep 12, 2025 · NAI
Reviewing Multisource Manufacturing LLC 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.
Or check Multisource Manufacturing LLC yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.
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 | 6 | Nov 8, 2026 | Newest record Oct 28, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Sep 12, 2025 | Longmont, CO | Devices | No Action Indicated (NAI) | 3010009632 |
| Dec 17, 2021 | Fridley, MN | Devices | Voluntary Action Indicated (VAI) | 3011604145 |
| Nov 8, 2017 | Longmont, CO | Devices | Voluntary Action Indicated (VAI) | 3010009632 |
| Feb 9, 2017 | Ramsey, MN | Devices | No Action Indicated (NAI) | 3004181214 |
| Nov 8, 2014 | Longmont, CO | Devices | No Action Indicated (NAI) | 3010009632 |
| Dec 12, 2008 | Ramsey, MN | Devices | No Action Indicated (NAI) | 3004181214 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3010009632 | Longmont, CO | 3 | Sep 12, 2025 |
| FEI 3011604145 | Fridley, MN | 1 | Dec 17, 2021 |
| FEI 3004181214 | Ramsey, MN | 2 | Feb 9, 2017 |