# FDA Inspection 917904 - Themogenesis Corp. - March 13, 2015

Source: https://www.keypedia.com/records/fda_inspections/themogenesis-corp/92984e47-a59d-4eda-a26d-7ceb0324fb79
Source feed: FDA_Inspections

> FDA Inspection 917904 for Themogenesis Corp. on March 13, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 917904
- Company Name: Themogenesis Corp.
- Inspection Date: 2015-03-13
- 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 917904 - 2015-03-13](https://www.keypedia.com/records/fda_inspections/themogenesis-corp/596495d4-528b-402f-9397-60e88caec862)
- [FDA Inspection 745069 - 2011-08-29](https://www.keypedia.com/records/fda_inspections/themogenesis-corp/0f01797d-95c9-4b0e-b3dd-aa825f931a32)
- [FDA Inspection 745069 - 2011-08-29](https://www.keypedia.com/records/fda_inspections/themogenesis-corp/9f12ce67-f766-4d5e-afd8-121ed6885ca4)

Company: https://www.keypedia.com/companies/themogenesis-corp/8caa0e47-7cc8-4c31-8109-e88cc1dd5047

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