# FDA Inspection 866732 - D3 Radiation Planning - February 20, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/d3-radiation-planning/d4262aac-f1e9-435e-8ac3-e2507a27bba2
Source feed: FDA_Inspections

> FDA Inspection 866732 for D3 Radiation Planning on February 20, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 866732
- Company Name: D3 Radiation Planning
- Inspection Date: 2014-02-20
- 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 866732 - 2014-02-20](https://www.globalkeysolutions.net/records/fda_inspections/d3-radiation-planning/42011f67-1d99-4adc-9e17-1a3c56fa85fc)
- [FDA Inspection 725911 - 2011-05-19](https://www.globalkeysolutions.net/records/fda_inspections/d3-radiation-planning/47d9709a-e28e-4668-ab7a-bef49a9cf31a)
- [FDA Inspection 725911 - 2011-05-19](https://www.globalkeysolutions.net/records/fda_inspections/d3-radiation-planning/db72721d-0a85-42aa-9671-be8a2c273602)

Company: https://www.globalkeysolutions.net/companies/d3-radiation-planning/454f0393-b432-43ab-b5b8-754eedd9ae62

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