FDA Inspection
VitalDyne, IncVitalDyne, Inc – FDA Inspection, Jun 24, 2014
Record Details
This FDA Inspection record concerns VitalDyne, Inc, with an inspection on June 24, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- VitalDyne, Inc
- Inspection Date
- June 24, 2014
- Product Type
- Devices
View Company Profile
ID · 9c32e548-8e22-401d-98ee-d92654d394da
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 899983
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of VitalDyne, Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| December 21, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 25, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 26, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 11, 2008 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for VitalDyne, Inc
- FDA Inspection 1227529 - 2023-12-21
- FDA Inspection 1048182 - 2018-01-25
- FDA Inspection 726603 - 2011-05-26
- FDA Inspection 551121 - 2008-12-11
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