FDA Inspection
Cardiox CorporationCardiox Corporation – FDA Inspection, Oct 30, 2013
Record Details
This FDA Inspection record concerns Cardiox Corporation, with an inspection on October 30, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Cardiox Corporation
- Inspection Date
- October 30, 2013
- Product Type
- Devices
View Company Profile
ID · 4f0b10ef-5520-4fd7-8274-208075a83c8f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 854394
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Cardiox Corporation
1| Date | Classification | Office | Project area |
|---|---|---|---|
| December 18, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Cardiox Corporation
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