# FDA Inspection 905723 - James Swain, MD - November 25, 2014

Source: https://www.keypedia.com/records/fda_inspections/james-swain-md/1283ba21-39f1-4aa6-8d3e-d4a0b5bd6790
Source feed: FDA_Inspections

> FDA Inspection 905723 for James Swain, MD on November 25, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 905723
- Company Name: James Swain, MD
- Inspection Date: 2014-11-25
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1127235 - 2020-08-07](https://www.keypedia.com/records/fda_inspections/james-swain-md/0becb44e-4fa6-41ee-a8f2-859557167858)

Company: https://www.keypedia.com/companies/james-swain-md/e6bab717-21be-4eb6-9ca8-406e18986ee4

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