# George King Bio-Medical, Inc. – FDA Inspection, Oct 27, 2016

Source: https://www.keypedia.com/records/fda_inspections/george-king-bio-medical-inc/c5d96a7f-5ed9-4f85-987c-569617ec842d
Source feed: FDA_Inspections

> FDA inspection 991776 of George King Bio-Medical, Inc., October 27, 2016. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 991776
- Company Name: George King Bio-Medical, Inc.
- Inspection Date: 2016-10-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1276234 - 2025-07-16
- FDA Inspection 1181783 - 2022-10-13
- [FDA Inspection 1024197 - 2017-09-06](https://www.keypedia.com/records/fda_inspections/george-king-bio-medical-inc/73e801d4-8e85-4261-91b3-118eadfa7b35)
- FDA Inspection 903607 - 2014-11-13
- FDA Inspection 803190 - 2012-10-16

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/amy-e-devine/7c46c4a4-99b2-4478-ab67-f0f70b36a4ce)
- [Company Rep](https://www.keypedia.com/people/karen-m-montgomery/ee91b1bb-8d51-4fdc-bee5-949441136e59)
- Issuing Officer

Company: https://www.keypedia.com/companies/george-king-bio-medical-inc/d086651c-4359-41cd-b4a0-b806ced03633

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7