# FDA Inspection 719170 - Timothy Murphy, M.D. - March 22, 2011

Source: https://www.keypedia.com/records/fda_inspections/timothy-murphy-md/a4c7ad9b-69ec-4851-9995-ebfc36cfef56
Source feed: FDA_Inspections

> FDA Inspection 719170 for Timothy Murphy, M.D. on March 22, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 719170
- Company Name: Timothy Murphy, M.D.
- Inspection Date: 2011-03-22
- 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/timothy-murphy-md/130b3b8e-cead-40d8-bbb8-6d24bd8ff302

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