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 3010490167.
Edge Pharma, LLC
Colchester, Vermont, United States
Issue DateApril 12, 2017
FEI Number3010490167
CountryUnited States
Status
No Warning Letter
Product Type
Outsourcing Facility
Establishment Type
Outsourcing Facility
Edge Pharma, LLC FDA Form 483, Colchester, Vermont, April 12, 2017
