FDA Inspection
CAO Group, Inc.CAO Group, Inc. – FDA Inspection, Aug 21, 2009
Record Details
This FDA Inspection record concerns CAO Group, Inc., with an inspection on August 21, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- CAO Group, Inc.
- Inspection Date
- August 21, 2009
- Product Type
- Devices
View Company Profile
ID · e05a62af-b001-44bf-a4c0-d6ff73f92bbd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 606759
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 820.198(a)General
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of CAO Group, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| July 8, 2025 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
| June 5, 2019 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| May 7, 2018 | OAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 25, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 26, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for CAO Group, Inc.
- FDA Inspection 1275079 - 2025-07-08
- FDA Inspection 1091932 - 2019-06-05
- FDA Inspection 1050998 - 2018-05-07
- FDA Inspection 967548 - 2016-03-25
- FDA Inspection 830062 - 2013-04-26
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