FDA 483 - Aesculap Inc - October 30, 2019
FDA 483 for Aesculap Inc on October 30, 2019. Product: device. Access full analysis and detailed observations.
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FDA 483 for Aesculap Inc on October 30, 2019. Product: device. Access full analysis and detailed observations.
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Company
Aesculap IncInspection Date
October 30, 2019
Product Type
device
ID: ce23b678-4e21-4660-9a07-aeb4b4cd0ec2
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