Source: FDA, document on fileFDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3008364285.
Jubilant Draximage Radiopharmacies Inc
Kansas City, Missouri, United States
Issue DateSeptember 19, 2017
FEI Number3008364285
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
Jubilant Draximage Radiopharmacies Inc FDA Form 483, Kansas City, Missouri, September 19, 2017
