# FDA Inspection 600075 - Kristin Ellison - June 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/kristin-ellison/ebb57d89-f068-42ae-b881-0eb2e8727b0c
Source feed: FDA_Inspections

> FDA Inspection 600075 for Kristin Ellison on June 30, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 600075
- Company Name: Kristin Ellison
- Inspection Date: 2009-06-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/kristin-ellison/742a9155-27b0-452c-b4a4-91a0a6fced04

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