# FDA Inspection 992521 - Timothy K. Amukele, MD - November 17, 2016

Source: https://www.keypedia.com/records/fda_inspections/timothy-k-amukele-md/890179e1-3e7b-4003-925b-81a6fa899761
Source feed: FDA_Inspections

> FDA Inspection 992521 for Timothy K. Amukele, MD on November 17, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 992521
- Company Name: Timothy K. Amukele, MD
- Inspection Date: 2016-11-17
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 952382 - 2015-12-09](https://www.keypedia.com/records/fda_inspections/timothy-k-amukele-md/13905603-6625-4eeb-bd71-40653d525506)

Company: https://www.keypedia.com/companies/timothy-k-amukele-md/6e482a4d-fecc-4ffd-9b8a-d94f68d4abba

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