FDA Inspection
Cerenovus, Inc.Cerenovus, Inc. – FDA Inspection, Sep 21, 2016
Record Details
This FDA Inspection record concerns Cerenovus, Inc., with an inspection on September 21, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Cerenovus, Inc.
- Inspection Date
- September 21, 2016
- Product Type
- Devices
View Company Profile
ID · acbaaf18-bd29-4ad5-8f56-fc3e8dc5004e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 985968
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Cerenovus, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| November 5, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 27, 2011 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| March 4, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 17, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 17, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Cerenovus, Inc.
- FDA Inspection 855739 - 2013-11-05
- FDA Inspection 746797 - 2011-09-27
- FDA Inspection 712819 - 2011-03-04
- FDA Inspection 673154 - 2010-06-17
- FDA Inspection 628600 - 2009-11-17
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