# FDA Inspection 651933 - Dio Corporation - February 11, 2010

Source: https://www.keypedia.com/records/fda_inspections/dio-corporation/2cb049f8-1a3a-4dd2-8fc0-52cacc4fbe13
Source feed: FDA_Inspections

> FDA Inspection 651933 for Dio Corporation on February 11, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 651933
- Company Name: Dio Corporation
- Inspection Date: 2010-02-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 651933 - 2010-02-11](https://www.keypedia.com/records/fda_inspections/dio-corporation/69126691-b2e5-4446-9595-8e39b7fdc3c6)

Company: https://www.keypedia.com/companies/dio-corporation/fcaab9eb-3e09-4607-b87a-000eb5a9294b

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