FDA Warning Letter — Andapharm, LLC

Case 566492 — FEI 3005000348

The FDA took a Warning Letter action against Andapharm, LLC on February 28, 2019 (Fort Lauderdale, FL). The action was issued by CDER and concerns drugs products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Andapharm, LLC
Date
February 28, 2019
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
Fort Lauderdale, FL (United States)