Aspire Bariatrics, Inc.
Aspire Bariatrics, Inc. has 0 FDA recalls, 3 inspections, 2 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Aug 31, 2017 · VAI
- Latest 510(k)
- Nov 13, 2018
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 2 | Oct 4, 2026 | Not stated | Current |
| Inspections | 3 | Oct 25, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Aug 31, 2017 | Exton, PA | Devices | Voluntary Action Indicated (VAI) | 3009595931 |
| Apr 19, 2016 | Exton, PA | Devices | Voluntary Action Indicated (VAI) | 3009595931 |
| Feb 18, 2015 | Exton, PA | Devices | No Action Indicated (NAI) | 3009595931 |