FDA Inspection 1029025 — Greenway, Frank L., MD

Greenway, Frank L., MD — FEI 3004730619

The FDA completed an inspection of Greenway, Frank L., MD on September 21, 2017 in Baton Rouge, LA. 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
September 21, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Baton Rouge, LA (United States)

Additional Details

Clinical Investigator (CI)