FDA Inspection
Hemagen Diagnostics IncHemagen Diagnostics Inc – FDA Inspection, Dec 20, 2012
Record Details
This FDA Inspection record concerns Hemagen Diagnostics Inc, with an inspection on December 20, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Hemagen Diagnostics Inc
- Inspection Date
- December 20, 2012
- Product Type
- Devices
View Company Profile
ID · 7e05ce43-8147-4113-97e7-05b629a63144
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 812190
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Hemagen Diagnostics Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| May 14, 2026 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 14, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 10, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 10, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 25, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Hemagen Diagnostics Inc
- FDA Inspection 1317040 - 2026-05-14
- FDA Inspection 1208393 - 2023-06-14
- FDA Inspection 1037233 - 2018-01-10
- FDA Inspection 918077 - 2015-03-10
- FDA Inspection 677299 - 2010-08-25
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