# FDA Inspection 1010158 - James C. Roberts, M.D. - April 07, 2017

Source: https://www.keypedia.com/records/fda_inspections/james-c-roberts-md/3a406e9c-bcf2-47d7-9716-5557d6fb40d6
Source feed: FDA_Inspections

> FDA Inspection 1010158 for James C. Roberts, M.D. on April 07, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1010158
- Company Name: James C. Roberts, M.D.
- Inspection Date: 2017-04-07
- 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/james-c-roberts-md/be33623d-1703-4d3b-81ea-46a1fee3efb8

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