FDA Inspection 822299 - Aesculap Inc - March 12, 2013

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Record Details

This FDA Inspection record concerns Aesculap Inc, with an inspection on March 12, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Aesculap Inc
Inspection Date: March 12, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b0482442-2513-47df-bfd8-9752c227312b

Violation Codes2

21 CFR 812.140(b)(2)21 CFR 812.140(b)(3)

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