# James C. Roberts, M.D. – FDA Inspection, Apr 7, 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 of James C. Roberts, M.D., April 07, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 50 and 812. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Officers

- [Investigator](https://www.keypedia.com/people/richard-w-berning/4637e321-8803-4fcf-911f-bbc810c3487d)

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