FDA Inspection 952382 — Timothy K. Amukele, MD

Timothy K. Amukele, MD — FEI 3011916235

The FDA completed an inspection of Timothy K. Amukele, MD on Dec 9, 2015 in Baltimore, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 9, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Baltimore, MD (United States)

Additional Details

Clinical Investigator (CI)