# FDA Inspection 553822 - Electromed, Inc. - December 11, 2008

Source: https://www.keypedia.com/records/fda_inspections/electromed-inc/4ce1f036-27ad-4dcb-8d12-41141a9f2e60
Source feed: FDA_Inspections

> FDA Inspection 553822 for Electromed, Inc. on December 11, 2008. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 553822
- Company Name: Electromed, Inc.
- Inspection Date: 2008-12-11
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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