# FDA Inspection 676571 - Daniel A. Potter, M.D. - August 19, 2010

Source: https://www.keypedia.com/records/fda_inspections/daniel-a-potter-md/7221f7d7-4dad-4ddc-a0df-aa39ded2a318
Source feed: FDA_Inspections

> FDA Inspection 676571 for Daniel A. Potter, M.D. on August 19, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 676571
- Company Name: Daniel A. Potter, M.D.
- Inspection Date: 2010-08-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 594160 - 2009-06-30](https://www.keypedia.com/records/fda_inspections/daniel-a-potter-md/9cc9b984-0068-47a0-b2fb-699b421f74f7)

Company: https://www.keypedia.com/companies/daniel-a-potter-md/44a2b457-3e5f-4abd-bf1a-80eed6867330

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