FDA Warning Letter — Jubilant Draximage Radiopharmacies Inc

Case 480877 — FEI 3008364285

The FDA took a Warning Letter action against Jubilant Draximage Radiopharmacies Inc on March 10, 2016 (Kansas City, MO). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Jubilant Draximage Radiopharmacies Inc
Date
March 10, 2016
Fiscal Year
2016
Product Type
Drugs
Center
CDER
Location
Kansas City, MO (United States)