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 3011761882.
Curexa - East, LLC dba Curexa
Egg Harbor Township, New Jersey, United States
Issue DateOctober 10, 2020
FEI Number3011761882
CountryUnited States
Status
1 Related Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
Curexa - East, LLC dba Curexa FDA Form 483, Egg Harbor Township, New Jersey, October 10, 2020
