FDA inspection
Electromed, Inc.: FDA inspection ending Nov 7, 2002
FDA inspection 248089 · No Action Indicated (NAI) · New Prague, MN
Key facts
| Inspection ID | 248089 |
|---|---|
| Firm | Electromed, Inc. |
| FEI number | 3003007907 |
| Address | 502 6th Ave NW |
| City | New Prague |
| State | MN |
| ZIP | 56071-1134 |
| Fiscal year | 2003 |
| Inspection end date | Nov 7, 2002 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med 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