# FDA Inspection 675325 - Jeffrey Kenkel, Md - July 27, 2010

Source: https://www.keypedia.com/records/fda_inspections/jeffrey-kenkel-md/3cb367cd-c6b5-41cf-aa57-08faf372153a
Source feed: FDA_Inspections

> FDA Inspection 675325 for Jeffrey Kenkel, Md on July 27, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 675325
- Company Name: Jeffrey Kenkel, Md
- Inspection Date: 2010-07-27
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 912989 - 2015-02-13](https://www.keypedia.com/records/fda_inspections/jeffrey-kenkel-md/7731c92d-7e4e-4eb7-9cc7-a353a75b6086)

Company: https://www.keypedia.com/companies/jeffrey-kenkel-md/d5fccc99-71fa-4fd3-af97-815b6434fc61

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