FDA Inspection
Hemedex, Inc.Hemedex, Inc. – FDA Inspection, Mar 14, 2013
Record Details
This FDA Inspection record concerns Hemedex, Inc., with an inspection on March 14, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Hemedex, Inc.
- Inspection Date
- March 14, 2013
- Product Type
- Devices
View Company Profile
ID · 921222cf-516b-41db-97f3-39d5a0508ffb
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 822744
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Hemedex, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 19, 2026 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 17, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 5, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 10, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Hemedex, Inc.
- FDA Inspection 1333962 - 2026-08-19
- FDA Inspection 1207959 - 2023-02-17
- FDA Inspection 1028218 - 2017-10-05
- FDA Inspection 667620 - 2010-06-10
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