# TeraRecon, Inc. – FDA Inspection, Oct 23, 2012

Source: https://www.keypedia.com/records/fda_inspections/terarecon-inc/f83789b0-59b0-47e5-9740-cd513d067f7e
Source feed: FDA_Inspections

> FDA inspection 803564 of TeraRecon, Inc., October 23, 2012. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 806 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803564
- Company Name: TeraRecon, Inc.
- Inspection Date: 2012-10-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 932214 - 2015-06-29](https://www.keypedia.com/records/fda_inspections/terarecon-inc/cb1aa190-cbd7-445a-9e1e-caea3b4aa809)
- [FDA Inspection 665677 - 2010-06-11](https://www.keypedia.com/records/fda_inspections/terarecon-inc/9ce3ea8e-ca2a-4f6a-b7ec-04f9827477b0)

Company: https://www.keypedia.com/companies/terarecon-inc/954290fa-f431-4540-a49b-40bb409f3fa5

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