# AEIOMed, Inc. – FDA Inspection, Jun 3, 2010

Source: https://www.keypedia.com/records/fda_inspections/aeiomed-inc/32e106d7-1e12-4b42-801b-c0d0657a8b51
Source feed: FDA_Inspections

> FDA inspection 667733 of AEIOMed, Inc., June 03, 2010. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 667733
- Company Name: AEIOMed, Inc.
- Inspection Date: 2010-06-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 790327 - 2012-07-11

Company: https://www.keypedia.com/companies/aeiomed-inc/b1ef21b7-7499-453a-9f8e-adb6cdb3b7e9

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