FDA Inspection
Pro-Dex IncPro-Dex Inc – FDA Inspection, Oct 12, 2011
Record Details
This FDA Inspection record concerns Pro-Dex Inc, with an inspection on October 12, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Pro-Dex Inc
- Inspection Date
- October 12, 2011
- Product Type
- Devices
View Company Profile
ID · c98c651b-5080-4944-b643-7776d9d16617
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 752142
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Pro-Dex Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 5, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Pro-Dex Inc
- FDA Inspection 894093 - 2014-09-05
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