# FDA Inspection 907852 - Vitaheat Medical - November 25, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/vitaheat-medical/12067487-f689-4c8b-b077-7fde725cf5f2
Source feed: FDA_Inspections

> FDA Inspection 907852 for Vitaheat Medical on November 25, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 907852
- Company Name: Vitaheat Medical
- Inspection Date: 2014-11-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1071338 - 2018-10-10](https://www.globalkeysolutions.net/records/fda_inspections/vitaheat-medical/e0a4efa2-63a8-474d-a41f-85e23439095e)
- [FDA Inspection 1071338 - 2018-10-10](https://www.globalkeysolutions.net/records/fda_inspections/vitaheat-medical/24152a84-ce29-46ed-81d2-8d317a72a007)
- [FDA Inspection 907852 - 2014-11-25](https://www.globalkeysolutions.net/records/fda_inspections/vitaheat-medical/c2b9ec41-2868-4010-a336-611c02b0bc61)

Company: https://www.globalkeysolutions.net/companies/vitaheat-medical/dbbe65db-80eb-4164-8b6b-53d1cfd444e4

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