# DIO USA – FDA Inspection, Nov 16, 2009

Source: https://www.keypedia.com/records/fda_inspections/dio-usa/70af05af-82ca-468c-9977-e483c329a8d2
Source feed: FDA_Inspections

> FDA inspection 627607 of DIO USA, November 16, 2009. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 803. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 627607
- Company Name: DIO USA
- Inspection Date: 2009-11-16
- 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: 2

## Related Documents

- [FDA Inspection 661058 - 2010-05-12](https://www.keypedia.com/records/fda_inspections/dio-usa/e9cd46c7-a113-4761-b3e3-9fba938695d9)

Company: https://www.keypedia.com/companies/dio-usa/00671082-a024-47e9-b139-1857c67e07ab

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