FDA inspection
Mainstream Medical Devices: FDA inspection ending May 29, 2026
FDA inspection 1322838 · No Action Indicated (NAI) · Austin, TX
Key facts
| Inspection ID | 1322838 |
|---|---|
| Firm | Mainstream Medical Devices |
| FEI number | 3016112537 |
| Address | 3913 Todd Ln Ste 112 |
| City | Austin |
| State | TX |
| ZIP | 78744 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | May 29, 2026 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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