ARCH-Blandon 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 3007925235ARCH-Blandon
Blandon, Pennsylvania, United States
Issue DateFebruary 07, 2020
FEI Number3007925235
CountryUnited States
Status
No Warning LetterProduct Type
Devices