# FDA Inspection 1026766 - James Joye, D.O. - March 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/james-joye-do/7d174e6b-abda-45c5-8f95-c296491650d1
Source feed: FDA_Inspections

> FDA Inspection 1026766 for James Joye, D.O. on March 31, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026766
- Company Name: James Joye, D.O.
- Inspection Date: 2017-03-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/james-joye-do/33bdc8f4-dbc8-468c-a374-4d1767757c24

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