# Hiossen Inc. – FDA Inspection, May 16, 2012

Source: https://www.keypedia.com/records/fda_inspections/hiossen-inc/e3aa3b86-da32-4ec5-8bc1-66c485a6d1fb
Source feed: FDA_Inspections

> FDA inspection 781029 of Hiossen Inc., May 16, 2012. Classification: Official Action Indicated (OAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 781029
- Company Name: Hiossen Inc.
- Inspection Date: 2012-05-16
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1007913 - 2017-04-12](https://www.keypedia.com/records/fda_inspections/hiossen-inc/dd809078-dc01-4693-922a-8058a0426732)
- FDA Inspection 831555 - 2013-04-18

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

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