# FDA Inspection 800071 - Jeffrey W. Moses, MD - October 05, 2012

Source: https://www.keypedia.com/records/fda_inspections/jeffrey-w-moses-md/1c221963-898e-4291-9fdd-31364c41a011
Source feed: FDA_Inspections

> FDA Inspection 800071 for Jeffrey W. Moses, MD on October 05, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 800071
- Company Name: Jeffrey W. Moses, MD
- Inspection Date: 2012-10-05
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1225706 - 2023-12-14](https://www.keypedia.com/records/fda_inspections/jeffrey-w-moses-md/cd2e789b-51bd-4f8b-bd71-2d0fe93b4f81)

Company: https://www.keypedia.com/companies/jeffrey-w-moses-md/ca27f066-ad90-431c-9e46-b27a6b74b084

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