# FDA Inspection 896792 - Hansol Medical - July 31, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/hansol-medical/1a4815ce-cb3a-4578-a9b5-104a938d2c39
Source feed: FDA_Inspections

> FDA Inspection 896792 for Hansol Medical on July 31, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 896792
- Company Name: Hansol Medical
- Inspection Date: 2014-07-31
- 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 1037310 - 2017-11-09](https://www.globalkeysolutions.net/records/fda_inspections/hansol-medical/8eb10d17-5b7c-4bb1-8372-03344183fa39)
- [FDA Inspection 896792 - 2014-07-31](https://www.globalkeysolutions.net/records/fda_inspections/hansol-medical/44e8631f-5b59-433f-aa02-0790527f409f)

Company: https://www.globalkeysolutions.net/companies/hansol-medical/9a7289bd-cdb9-42cf-b718-04622d608341

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