FDA inspection
Electromed, Inc.: FDA inspection ending Feb 12, 2026
FDA inspection 1303288 · Voluntary Action Indicated (VAI) · New Prague, MN
Key facts
| Inspection ID | 1303288 |
|---|---|
| Firm | Electromed, Inc. |
| FEI number | 3003007907 |
| Address | 502 6th Ave NW |
| City | New Prague |
| State | MN |
| ZIP | 56071 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Feb 12, 2026 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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