FDA Inspection 1039070 — Melissa Gilliam

Melissa Gilliam — FEI 3013911075

The FDA completed an inspection of Melissa Gilliam on Dec 14, 2017 in Chicago, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 14, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Chicago, IL (United States)

Additional Details

Clinical Investigator (CI)