FDA Warning Letter — Jubilant Draximage Radiopharmacies Inc

Case 480877 — FEI 3008364285

The FDA took a Warning Letter action against Jubilant Draximage Radiopharmacies Inc on Mar 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
Mar 10, 2016
Fiscal Year
2016
Product Type
Drugs
Center
CDER
Location
Kansas City, MO (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.