# FDA Inspection 631841 - Timothy Bunchman, M.D. - November 06, 2009

Source: https://www.keypedia.com/records/fda_inspections/timothy-bunchman-md/2a2fe73c-1911-45dd-a6f9-33a04aa37306
Source feed: FDA_Inspections

> FDA Inspection 631841 for Timothy Bunchman, M.D. on November 06, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 631841
- Company Name: Timothy Bunchman, M.D.
- Inspection Date: 2009-11-06
- 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-bunchman-md/09f16c0b-675e-453f-8f40-e22070298c03

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