FDA Inspection 791638 — Keith A. Aqua, M.D.

Keith A. Aqua, M.D. — FEI 3005625732

The FDA completed an inspection of Keith A. Aqua, M.D. on July 13, 2012 in Boynton Beach, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 13, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Boynton Beach, FL (United States)

Additional Details

Clinical Investigator (CI)