# Kathleen Gibson, M.D. – FDA Inspection, Nov 21, 2014

Source: https://www.keypedia.com/records/fda_inspections/kathleen-gibson-md/e4e5a17c-7bc4-46b7-8533-26b4e7fde061
Source feed: FDA_Inspections

> FDA inspection 901733 of Kathleen Gibson, M.D., November 21, 2014. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 901733
- Company Name: Kathleen Gibson, M.D.
- Inspection Date: 2014-11-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 859729 - 2013-11-08

Company: https://www.keypedia.com/companies/kathleen-gibson-md/31c24280-f98d-47ea-826b-a644c7d61cf3

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