# FDA Inspection 1046733 - Jeffery Hoggard, MD - March 21, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/jeffery-hoggard-md/2608e478-0e78-4af8-8e4b-d301b48db1d6
Source feed: FDA_Inspections

> FDA Inspection 1046733 for Jeffery Hoggard, MD on March 21, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1046733
- Company Name: Jeffery Hoggard, MD
- Inspection Date: 2018-03-21
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1012198 - 2017-05-12](https://www.globalkeysolutions.net/records/fda_inspections/jeffery-hoggard-md/52526b4f-9446-480b-84c4-8002eb48c784)
- [FDA Inspection 869797 - 2014-03-13](https://www.globalkeysolutions.net/records/fda_inspections/jeffery-hoggard-md/ce8db833-e44f-42fb-8e4c-26f76559ebfa)

Company: https://www.globalkeysolutions.net/companies/jeffery-hoggard-md/8976a69b-b152-40fe-aee6-10d1467bee2b

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