FDA Inspection 1037411 — Kelly Taylor

Kelly Taylor — FEI 3013982624

The FDA completed an inspection of Kelly Taylor on Dec 8, 2017 in Ocoee, FL. 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 8, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Ocoee, FL (United States)

Additional Details

Clinical Investigator (CI)