# Hiossen Inc. – FDA Inspection, Apr 12, 2017

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

> FDA inspection 1007913 of Hiossen Inc., April 12, 2017. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 831555 - 2013-04-18
- [FDA Inspection 781029 - 2012-05-16](https://www.keypedia.com/records/fda_inspections/hiossen-inc/e3aa3b86-da32-4ec5-8bc1-66c485a6d1fb)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/edward-d-mcdonald/69224613-2b96-426a-99dd-e1cfe5ff1713)

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