# FDA Inspection 1035602 - Theradome, Inc. - November 20, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/theradome-inc/666480f9-aace-480c-87bf-5e28c5a35888
Source feed: FDA_Inspections

> FDA Inspection 1035602 for Theradome, Inc. on November 20, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1035602
- Company Name: Theradome, Inc.
- Inspection Date: 2017-11-20
- 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 1035602 - 2017-11-20](https://www.globalkeysolutions.net/records/fda_inspections/theradome-inc/506854b7-7fce-4a55-a2dc-aa7dc172c04f)

Company: https://www.globalkeysolutions.net/companies/theradome-inc/062c7ab4-b413-421c-ad37-6ee5d7f8068a

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