FDA Inspection
Cerenovus, Inc.Cerenovus, Inc. – FDA Inspection, Mar 4, 2011
Record Details
This FDA Inspection record concerns Cerenovus, Inc., with an inspection on March 4, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Cerenovus, Inc.
- Inspection Date
- March 4, 2011
- Product Type
- Devices
View Company Profile
ID · e3b52dca-480c-4ba8-866b-20f07a2d2fff
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 712819
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Cerenovus, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 21, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| 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 |
| 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 985968 - 2016-09-21
- FDA Inspection 855739 - 2013-11-05
- FDA Inspection 746797 - 2011-09-27
- FDA Inspection 673154 - 2010-06-17
- FDA Inspection 628600 - 2009-11-17
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