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 3000210731.
Eon Labs Inc
Wilson, North Carolina, United States
Issue DateJuly 11, 2015
FEI Number3000210731
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Drug Manufacturer
Eon Labs Inc FDA Form 483, Wilson, North Carolina, July 11, 2015
