FDA Inspection
Omni-Guide Holdings, Inc.Omni-Guide Holdings, Inc. – FDA Inspection, Nov 15, 2012
Record Details
This FDA Inspection record concerns Omni-Guide Holdings, Inc., with an inspection on November 15, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Omni-Guide Holdings, Inc.
- Inspection Date
- November 15, 2012
- Product Type
- Devices
View Company Profile
ID · 8a918bc0-57a2-4b34-9892-ddbd2ade9a72
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 807195
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Omni-Guide Holdings, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| August 19, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 2, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 5, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 24, 2014 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| February 13, 2012 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Omni-Guide Holdings, Inc.
- FDA Inspection 1177895 - 2022-08-19
- FDA Inspection 1009910 - 2017-05-02
- FDA Inspection 997999 - 2017-01-05
- FDA Inspection 888872 - 2014-07-24
- FDA Inspection 765565 - 2012-02-13
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