CorneaGen, LLC Form 483 Details
Form 483Source: FDA Data DashboardFDA has published this inspection and the number of observations cited. The form itself has not been released yet, which usually takes six to twelve months.
Check this firm on FDA, establishment 3009122697CorneaGen, LLC
South San Francisco, California, United States
Issue DateJuly 29, 2022
FEI Number3009122697
CountryUnited States
Status
No Warning LetterProduct Type
Biologics