FDA 483_RESPONSE - Biomet, Inc. - November 22, 2016

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Record Details

This 483 RESPONSE record concerns Biomet, Inc., with an inspection on November 22, 2016, issued by the Office of Health Technology 5 (Neurological and Physical Medicine Devices), covering devices.

Company: Biomet, Inc.
Inspection Date: November 22, 2016
Product Type: Devices
Office: Office of Health Technology 5 (Neurological and Physical Medicine Devices)
People: Joseph R. Strelnik ( Investigator )
Barbara J. Cassens (Director )
Art O. Czabaniuk (Program Division Director)
Thomas A. Peter (Medical Device Senior Operations Officer at FDA)
Jeff Kim (US Agent)

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ID · 159e464e-90ad-4ff9-a4d7-e4c8086af1be

Violation Codes3

FD&C Act 801(a)(3)21 CFR 82021 CFR 820.5

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