# FDA Inspection 1038513 - Hiossen Inc. - April 24, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/hiossen-inc/6c2920e7-6c58-4424-9703-46b4cfcbb7a7
Source feed: FDA_Inspections

> FDA Inspection 1038513 for Hiossen Inc. on April 24, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038513
- Company Name: Hiossen Inc.
- Inspection Date: 2017-04-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/hiossen-inc/5913cd53-b64c-4d14-a379-c5812e63a60d

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