FDA Inspection 998465 - B. Braun Aesculap Japan Co., Ltd. - December 01, 2016

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Record Details

This FDA Inspection record concerns B. Braun Aesculap Japan Co., Ltd., with an inspection on December 1, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: B. Braun Aesculap Japan Co., Ltd.
Inspection Date: December 1, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 12b69b3b-2b21-4367-a0d0-bac697be29fc