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FDA Inspection 934705 — Electromed, Inc.

Electromed, Inc. — FEI 3003007907

The FDA completed an inspection of Electromed, Inc. on July 10, 2015 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
July 10, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
New Prague, MN (United States)

Facility

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FDA data resources