# FDA Inspection 1007913 - Hiossen Inc. - April 12, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/hiossen-inc/dd809078-dc01-4693-922a-8058a0426732
Source feed: FDA_Inspections

> FDA Inspection 1007913 for Hiossen Inc. on April 12, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1007913
- Company Name: Hiossen Inc.
- Inspection Date: 2017-04-12
- 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 1007913 - 2017-04-12](https://www.globalkeysolutions.net/records/fda_inspections/hiossen-inc/d3a18ad9-be6e-4cba-8113-aed0dc5b7b90)
- [FDA Inspection 831555 - 2013-04-18](https://www.globalkeysolutions.net/records/fda_inspections/hiossen-inc/28fa54cd-714e-4d94-b50d-8a493ff2f792)
- [FDA Inspection 781029 - 2012-05-16](https://www.globalkeysolutions.net/records/fda_inspections/hiossen-inc/44bb7fcf-3d85-43b9-ab69-9c59b728dc6f)
- [FDA Inspection 781029 - 2012-05-16](https://www.globalkeysolutions.net/records/fda_inspections/hiossen-inc/e3aa3b86-da32-4ec5-8bc1-66c485a6d1fb)

Company: https://www.globalkeysolutions.net/companies/hiossen-inc/d384b90a-dcb2-4020-acd1-2195a0ef67d9

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