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483 RESPONSE
•Biomet, Inc.•November 22, 2016

Biomet, Inc. – FDA 483 Response, Nov 22, 2016

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
  • Art O. Czabaniuk (Program Division Director)
  • Thomas A. Peter (Medical Device Senior Operations Officer at FDA)
  • Joseph R. Strelnik ( Investigator )
  • Suyang Qin ( Investigator )
  • David Sencabaugh
View Company Profile

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

Violation Codes3
21 CFR 82021 CFR 820.5FD&C Act 801(a)(3)

Full citation text and observation details available on the Dashboard.

Other documents for Biomet, Inc.
  • 483 - 2023-11-09November 9, 2023
  • 483 - 2020-01-30January 30, 2020
  • 483 - 2018-04-24April 24, 2018
  • 483 - 2017-10-16October 16, 2017
  • 483 - 2016-11-22November 22, 2016

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