# FDA Inspection 791127 - Theg, Inc. - June 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/theg-inc/32ad4116-204d-4cff-baa8-090e295bb622
Source feed: FDA_Inspections

> FDA Inspection 791127 for Theg, Inc. on June 20, 2012. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 791127
- Company Name: Theg, Inc.
- Inspection Date: 2012-06-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1026149 - 2017-08-16](https://www.keypedia.com/records/fda_inspections/theg-inc/9bff778c-b2af-4874-8ecc-210f96045076)
- [FDA Inspection 857464 - 2013-11-15](https://www.keypedia.com/records/fda_inspections/theg-inc/2f03f419-989d-4858-a87e-f0d2ba2499a3)
- [FDA Inspection 791127 - 2012-06-20](https://www.keypedia.com/records/fda_inspections/theg-inc/c2e1c784-15a3-4478-aa42-a68a51871990)
- [FDA Inspection 620022 - 2009-10-13](https://www.keypedia.com/records/fda_inspections/theg-inc/3efdd8f5-2d45-4094-9ddc-d5d51d4693fe)

Company: https://www.keypedia.com/companies/theg-inc/9d7b283b-8101-49e5-9675-928b65401115

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