FDA Warning Letter — Keith A. Aqua, M.D.

Case 436187 — FEI 3005625732

The FDA took a Warning Letter action against Keith A. Aqua, M.D. on September 2, 2014 (Boynton Beach, FL). The action was issued by CDER and concerns drugs products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Keith A. Aqua, M.D.
Date
September 2, 2014
Fiscal Year
2014
Product Type
Drugs
Center
CDER
Location
Boynton Beach, FL (United States)