FDA Inspection 752313 — Electromed, Inc.
The FDA completed an inspection of Electromed, Inc. on November 7, 2011 in New Prague, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 7, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- New Prague, MN (United States)