# FDA Inspection 1195800 - Electromed, Inc. - January 13, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/electromed-inc/db601326-5018-455f-a2f6-d5efe11dfa42
Source feed: FDA_Inspections

> FDA Inspection 1195800 for Electromed, Inc. on January 13, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1195800
- Company Name: Electromed, Inc.
- Inspection Date: 2023-01-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1195800 - 2023-01-13](https://www.globalkeysolutions.net/records/fda_inspections/electromed-inc/4f586186-2889-4d49-9ed6-e85ca04bf5b3)
- [FDA Inspection 1042084 - 2017-12-15](https://www.globalkeysolutions.net/records/fda_inspections/electromed-inc/a883bdaa-535b-4d37-b521-32a70172eb14)
- [FDA Inspection 934705 - 2015-07-10](https://www.globalkeysolutions.net/records/fda_inspections/electromed-inc/8621dacc-bf4f-45cc-a8cb-bc8327b9b216)
- [FDA Inspection 752313 - 2011-11-07](https://www.globalkeysolutions.net/records/fda_inspections/electromed-inc/31a2351b-f79a-4ee0-a5bb-ba39a4c51672)
- [FDA Inspection 553822 - 2008-12-11](https://www.globalkeysolutions.net/records/fda_inspections/electromed-inc/4ce1f036-27ad-4dcb-8d12-41141a9f2e60)

Company: https://www.globalkeysolutions.net/companies/electromed-inc/2e0611e6-8d86-449f-92c2-322112b6169a

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7