FDA Inspection 1014963 — Raymond De La Rosa, M.D.

Raymond De La Rosa, M.D. — FEI 3007912583

The FDA completed an inspection of Raymond De La Rosa, M.D. on May 26, 2017 in Paducah, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 26, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Paducah, KY (United States)

Additional Details

Clinical Investigator (CI)