# FDA Inspection 892130 - Suni Medical Imaging - August 21, 2014

Source: https://www.keypedia.com/records/fda_inspections/suni-medical-imaging/759e2b49-fcc2-44fc-86b5-ca23b7fd6f0b
Source feed: FDA_Inspections

> FDA Inspection 892130 for Suni Medical Imaging on August 21, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 892130
- Company Name: Suni Medical Imaging
- Inspection Date: 2014-08-21
- 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 892130 - 2014-08-21](https://www.keypedia.com/records/fda_inspections/suni-medical-imaging/98140050-54fe-4bc3-9b69-352ef048b8c4)
- [FDA Inspection 614843 - 2009-09-22](https://www.keypedia.com/records/fda_inspections/suni-medical-imaging/b0eec335-45c3-47dd-b005-03efdcf439bc)
- [FDA Inspection 614843 - 2009-09-22](https://www.keypedia.com/records/fda_inspections/suni-medical-imaging/6dc0d684-0569-4f86-b6ce-a4d3115868b7)

Company: https://www.keypedia.com/companies/suni-medical-imaging/1c97c863-998f-4f4b-a525-6827058c95c1

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