# FDA Inspection 1016204 - John H. Joseph, M.D - June 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/john-h-joseph-md/a2965d9f-d4d0-48bd-b9e1-da1affd8ce02
Source feed: FDA_Inspections

> FDA Inspection 1016204 for John H. Joseph, M.D on June 28, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1016204
- Company Name: John H. Joseph, M.D
- Inspection Date: 2017-06-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1202752 - 2023-04-12](https://www.keypedia.com/records/fda_inspections/john-h-joseph-md/d735a998-6b4f-4e76-aaee-6eb75458a4a7)
- [FDA Inspection 1122362 - 2020-03-13](https://www.keypedia.com/records/fda_inspections/john-h-joseph-md/3efef27c-d1a9-4d21-9d45-8f68f406bbf9)
- [FDA Inspection 893898 - 2014-08-25](https://www.keypedia.com/records/fda_inspections/john-h-joseph-md/75579cc1-f90d-4b87-aaba-6eec686504cd)
- [FDA Inspection 615210 - 2009-09-23](https://www.keypedia.com/records/fda_inspections/john-h-joseph-md/df1a70c4-c772-4962-a166-e054e6869ba9)

Company: https://www.keypedia.com/companies/john-h-joseph-md/75e8219c-8cf8-492b-bb32-f737a4447fd6

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