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FDA Inspection
•Aesculap Inc•March 12, 2013

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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