# FDA Inspection 896761 - Imthera Medical Inc - September 09, 2014

Source: https://www.keypedia.com/records/fda_inspections/imthera-medical-inc/37f365eb-5ffc-420c-98d2-d01d7dc8e1e7
Source feed: FDA_Inspections

> FDA Inspection 896761 for Imthera Medical Inc on September 09, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 896761
- Company Name: Imthera Medical Inc
- Inspection Date: 2014-09-09
- 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 1052332 - 2018-03-08](https://www.keypedia.com/records/fda_inspections/imthera-medical-inc/1c51e5ec-e64d-484e-a43b-9ef3a45c1e74)
- [FDA Inspection 896761 - 2014-09-09](https://www.keypedia.com/records/fda_inspections/imthera-medical-inc/b2c7c07c-0841-4456-bc84-014697441775)

Company: https://www.keypedia.com/companies/imthera-medical-inc/2a5d2f5c-dbe5-434f-a732-c1714bf571d3

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