# FDA Inspection 901733 - Kathleen Gibson, M.D. - November 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 for Kathleen Gibson, M.D. on November 21, 2014. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 859729 - 2013-11-08](https://www.keypedia.com/records/fda_inspections/kathleen-gibson-md/e0d39e71-46a6-4af1-bfe0-6b66c85834ed)

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