FDA Inspection
Diacor, IncDiacor, Inc – FDA Inspection, Jun 19, 2013
Record Details
This FDA Inspection record concerns Diacor, Inc, with an inspection on June 19, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Diacor, Inc
- Inspection Date
- June 19, 2013
- Product Type
- Devices
View Company Profile
ID · ec5df3dc-96c9-4df3-a1e2-f6325281814b
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 836648
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Diacor, Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 8, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 17, 2010 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| June 25, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Diacor, Inc
- FDA Inspection 1024795 - 2017-09-08
- FDA Inspection 671010 - 2010-06-17
- FDA Inspection 592352 - 2009-06-25
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