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 3004483441.
Cantrell Drug Company
Little Rock, Arkansas, United States
Issue DateOctober 24, 2018
FEI Number3004483441
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
Cantrell Drug Company FDA Form 483, Little Rock, Arkansas, October 24, 2018
