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 3012039582.
Reliant Compounded Solutions Monroe, LLC
Monroe, Connecticut, United States
Issue DateApril 24, 2017
FEI Number3012039582
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
Reliant Compounded Solutions Monroe, LLC FDA Form 483, Monroe, Connecticut, April 24, 2017
