# FDA Inspection 705264 - Kevin Boylan, M.D. - January 07, 2011

Source: https://www.keypedia.com/records/fda_inspections/kevin-boylan-md/36bf3d6d-4ca1-4ec9-9b81-296093d1a5fa
Source feed: FDA_Inspections

> FDA Inspection 705264 for Kevin Boylan, M.D. on January 07, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 705264
- Company Name: Kevin Boylan, M.D.
- Inspection Date: 2011-01-07
- 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/kevin-boylan-md/290db7ed-8294-448c-ad4e-7bef13d89f0b

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