# FDA Inspection 695252 - ITC Nexus Dx - November 12, 2010

Source: https://www.keypedia.com/records/fda_inspections/itc-nexus-dx/97755a2c-4052-4265-b398-e11154cffe7b
Source feed: FDA_Inspections

> FDA Inspection 695252 for ITC Nexus Dx on November 12, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 695252
- Company Name: ITC Nexus Dx
- Inspection Date: 2010-11-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 695252 - 2010-11-12](https://www.keypedia.com/records/fda_inspections/itc-nexus-dx/d32aa5b0-f2f3-4c8d-8b62-aeef0f6be06b)
- [FDA Inspection 556414 - 2009-01-07](https://www.keypedia.com/records/fda_inspections/itc-nexus-dx/1c3e2276-c71f-4300-9514-00679d137cb4)
- [FDA Inspection 556414 - 2009-01-07](https://www.keypedia.com/records/fda_inspections/itc-nexus-dx/367309c9-faf8-4a71-b435-0f098a83ff0d)

Company: https://www.keypedia.com/companies/itc-nexus-dx/28632927-8b25-471b-ab9d-f94b8e7e286c

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