FDA Inspection 812433 — Delilah M. Burrowes

Delilah M. Burrowes — FEI 3009893771

The FDA completed an inspection of Delilah M. Burrowes on Jan 4, 2013 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
Jan 4, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Chicago, IL (United States)

Additional Details

Clinical Investigator (CI)