# FDA Inspection 1077880 - Arthur C. Lee, MD - January 16, 2019

Source: https://www.keypedia.com/records/fda_inspections/arthur-c-lee-md/07854f66-afbc-49a3-b8ac-6f8b6eaca62e
Source feed: FDA_Inspections

> FDA Inspection 1077880 for Arthur C. Lee, MD on January 16, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1077880
- Company Name: Arthur C. Lee, MD
- Inspection Date: 2019-01-16
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1198106 - 2023-02-16](https://www.keypedia.com/records/fda_inspections/arthur-c-lee-md/ce76c223-9ab8-48bd-a2cb-f1ca3c33b632)

Company: https://www.keypedia.com/companies/arthur-c-lee-md/526265a4-8f4c-4678-b66a-b70670fa125f

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