# FDA Inspection 851968 - Teratech Corporation - August 28, 2013

Source: https://www.keypedia.com/records/fda_inspections/teratech-corporation/fa6fc204-d8c9-4999-a43c-8c2b8582387c
Source feed: FDA_Inspections

> FDA Inspection 851968 for Teratech Corporation on August 28, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 851968
- Company Name: Teratech Corporation
- Inspection Date: 2013-08-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 740576 - 2011-08-05](https://www.keypedia.com/records/fda_inspections/teratech-corporation/75b066b0-7f24-4ac7-b5d9-14fda9d85ff9)
- [FDA Inspection 740576 - 2011-08-05](https://www.keypedia.com/records/fda_inspections/teratech-corporation/80a34e97-c26c-481f-a8db-d3161da5dfbf)

Company: https://www.keypedia.com/companies/teratech-corporation/efab230d-e183-4dff-a196-1dad8589d9fa

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