Limerick, Inc.
Limerick, Inc. has 0 FDA recalls, 5 inspections, 4 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Aug 15, 2025 · VAI
- Latest 510(k)
- Feb 20, 2015
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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 | 5 | Nov 10, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Aug 15, 2025 | Burbank, CA | Devices | Voluntary Action Indicated (VAI) | 3002297831 |
| Aug 26, 2021 | Burbank, CA | Devices | No Action Indicated (NAI) | 3002297831 |
| Feb 11, 2015 | Burbank, CA | Devices | No Action Indicated (NAI) | 3002297831 |
| Dec 7, 2012 | Burbank, CA | Devices | Voluntary Action Indicated (VAI) | 3002297831 |
| Feb 25, 2009 | Burbank, CA | Devices | No Action Indicated (NAI) | 3002297831 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3002297831 | Burbank, CA | 5 | Aug 15, 2025 |