# Electromed, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/electromed-inc/2e0611e6-8d86-449f-92c2-322112b6169a

> Inspection records and compliance data for Electromed, Inc. in New Prague, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Electromed, Inc.
- FEI Number: 3003007907
- City: New Prague
- State: Minnesota
- Country Name: United States
- Address Line 1: 502 6th Ave NW
- Zip Code: 56071

## Related Documents

- [483 - Electromed, Inc. - 2023-01-13](https://www.keypedia.com/records/483/electromed-inc/19f827b6-7dac-4558-b764-3930fa8df658) — source: FDA, date: January 13, 2023
- [FDA Inspection 1195800 - Electromed, Inc. - 2023-01-13](https://www.keypedia.com/records/fda_inspections/electromed-inc/4f586186-2889-4d49-9ed6-e85ca04bf5b3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2023
- [FDA Inspection 1195800 - Electromed, Inc. - 2023-01-13](https://www.keypedia.com/records/fda_inspections/electromed-inc/db601326-5018-455f-a2f6-d5efe11dfa42) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2023
- [FDA Inspection 1042084 - Electromed, Inc. - 2017-12-15](https://www.keypedia.com/records/fda_inspections/electromed-inc/a883bdaa-535b-4d37-b521-32a70172eb14) — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2017
- [FDA Inspection 934705 - Electromed, Inc. - 2015-07-10](https://www.keypedia.com/records/fda_inspections/electromed-inc/8621dacc-bf4f-45cc-a8cb-bc8327b9b216) — classification: No Action Indicated (NAI), source: FDA, date: July 10, 2015
- [FDA Inspection 752313 - Electromed, Inc. - 2011-11-07](https://www.keypedia.com/records/fda_inspections/electromed-inc/31a2351b-f79a-4ee0-a5bb-ba39a4c51672) — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2011
- [FDA Inspection 553822 - Electromed, Inc. - 2008-12-11](https://www.keypedia.com/records/fda_inspections/electromed-inc/4ce1f036-27ad-4dcb-8d12-41141a9f2e60) — classification: No Action Indicated (NAI), source: FDA, date: December 11, 2008

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