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 3005949964.
Catalent Indiana, LLC
Bloomington, Indiana, United States
Issue DateMay 01, 2018
FEI Number3005949964
CountryUnited States
Status
1 Related Warning Letter
Product Type
Drugs
Establishment Type
Active Pharmaceutical Ingredient Manufacturer
Catalent Indiana, LLC FDA Form 483, Bloomington, Indiana, May 1, 2018
