FDA Inspection
Cardia IncCardia Inc – FDA Inspection, May 18, 2011
Record Details
This FDA Inspection record concerns Cardia Inc, with an inspection on May 18, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Cardia Inc
- Inspection Date
- May 18, 2011
- Product Type
- Devices
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ID · f7d24380-f2cd-412b-9708-cd8327ef7ddd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 726443
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.75(a)Documentation
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Other FDA inspections of Cardia Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 2, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 19, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Cardia Inc
- FDA Inspection 971843 - 2016-05-02
- FDA Inspection 813176 - 2012-12-19
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