FDA Inspection 1026777 — Cesar Keller, MD

Cesar Keller, MD — FEI 1000306056

The FDA completed an inspection of Cesar Keller, MD on August 21, 2017 in Jacksonville, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 21, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Jacksonville, FL (United States)

Additional Details

Clinical Investigator (CI)