FDA Inspection 660506 — Kris A. Manlove-Simmons, M.D.

Kris A. Manlove-Simmons, M.D. — FEI 3007568124

The FDA completed an inspection of Kris A. Manlove-Simmons, M.D. on August 30, 2011 in Decatur, GA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 30, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Decatur, GA (United States)

Additional Details

Clinical Investigator (CI)