Aesculap Inc 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 2916714Aesculap Inc
Center Valley, Pennsylvania, United States
Issue DateAugust 11, 2021
FEI Number2916714
CountryUnited States
Status
No Warning LetterProduct Type
Devices