# FDA Inspection 624125 - Averion International, Inc. - October 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/averion-international-inc/7b5ff6af-d0a5-4e80-af55-b38fd78fa08a
Source feed: FDA_Inspections

> FDA Inspection 624125 for Averion International, Inc. on October 28, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 624125
- Company Name: Averion International, Inc.
- Inspection Date: 2009-10-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 547720 - 2008-11-19](https://www.keypedia.com/records/fda_inspections/averion-international-inc/d7a9ef82-4545-42c2-90a1-b3e30497ce5c)

Company: https://www.keypedia.com/companies/averion-international-inc/cf4d6481-bc0b-4efe-9782-6f003207ee58

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