FDA Inspection
George King Bio-Medical, Inc.George King Bio-Medical, Inc. – FDA Inspection, Oct 27, 2016
Record Details
This FDA Inspection record concerns George King Bio-Medical, Inc., with an inspection on October 27, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- People
- Amy E. Devine (FDA Associated Person)
- Karen M. Montgomery (Company Rep)
- Mary K. Concannon (Issuing Officer)
View Company Profile
ID · c5d96a7f-5ed9-4f85-987c-569617ec842d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 991776
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of George King Bio-Medical, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| July 16, 2025 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 13, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 6, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 13, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 16, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for George King Bio-Medical, Inc.
- FDA Inspection 1276234 - 2025-07-16
- FDA Inspection 1181783 - 2022-10-13
- FDA Inspection 1024197 - 2017-09-06
- FDA Inspection 903607 - 2014-11-13
- FDA Inspection 803190 - 2012-10-16
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