FDA Inspection
Hiossen Inc.Hiossen Inc. – FDA Inspection, May 16, 2012
Record Details
This FDA Inspection record concerns Hiossen Inc., with an inspection on May 16, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Hiossen Inc.
- Inspection Date
- May 16, 2012
- Product Type
- Devices
View Company Profile
ID · e3aa3b86-da32-4ec5-8bc1-66c485a6d1fb
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 781029
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Hiossen Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 12, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 18, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Hiossen Inc.
- FDA Inspection 1007913 - 2017-04-12
- FDA Inspection 831555 - 2013-04-18
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.