# FDA Inspection 803908 - ThermoGear Inc - October 19, 2012

Source: https://www.keypedia.com/records/fda_inspections/thermogear-inc/b1df0842-4e30-42ff-9a0a-64cc3b2a3211
Source feed: FDA_Inspections

> FDA Inspection 803908 for ThermoGear Inc on October 19, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803908
- Company Name: ThermoGear Inc
- Inspection Date: 2012-10-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 803908 - 2012-10-19](https://www.keypedia.com/records/fda_inspections/thermogear-inc/e27c027e-869d-472b-ae80-c4d1e1f56d7d)
- [FDA Inspection 701990 - 2010-12-03](https://www.keypedia.com/records/fda_inspections/thermogear-inc/ce3cc9e8-2d0a-4667-8586-534c87169b11)
- [FDA Inspection 701990 - 2010-12-03](https://www.keypedia.com/records/fda_inspections/thermogear-inc/cca469b7-115b-4726-9722-2af46d3792e8)

Company: https://www.keypedia.com/companies/thermogear-inc/0056462a-c8ad-4935-904c-e6a479cc4fa3

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