FDA Inspection 1087314 — Dr. Corby D. Ropp

Dr. Corby D. Ropp — FEI 3015144724

The FDA completed an inspection of Dr. Corby D. Ropp on March 22, 2019 in Camp Lejeune, NC. 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
March 22, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Camp Lejeune, NC (United States)

Additional Details

Clinical Investigator (CI)