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 3011501377.
Diamond Pharmacy, LLC
Houston, Montana, United States
Issue DateSeptember 01, 2016
FEI Number3011501377
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
Diamond Pharmacy, LLC FDA Form 483, Houston, Montana, September 1, 2016
