FDA Inspection
Cardea Technology, IncCardea Technology, Inc – FDA Inspection, Apr 29, 2011
Record Details
This FDA Inspection record concerns Cardea Technology, Inc, with an inspection on April 29, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Cardea Technology, Inc
- Inspection Date
- April 29, 2011
- Product Type
- Devices
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ID · f1dd2313-1495-47f3-9f9d-ecaa0570d1a4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 721953
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
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Other FDA inspections of Cardea Technology, Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 21, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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