FDA inspection
Mobia Medical Inc: FDA inspection ending Mar 19, 2026
FDA inspection 1308782 · Voluntary Action Indicated (VAI) · Lakeway, TX
Key facts
| Inspection ID | 1308782 |
|---|---|
| Firm | Mobia Medical Inc |
| FEI number | 3012309950 |
| Address | 2802 Flintrock Trce Ste 226 |
| City | Lakeway |
| State | TX |
| ZIP | 78738 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Mar 19, 2026 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data