FDA Inspection 1042084 — Electromed, Inc.
The FDA completed an inspection of Electromed, Inc. on December 15, 2017 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
- December 15, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- New Prague, MN (United States)