Biomet, Inc.

Form 483FOIA Uncovered

Warsaw, IndianaFEI 1825034Issued November 09, 2023

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1825034.

ObservationsNot available

Issue DateNovember 09, 2023

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: Biomet, Inc.
Location: Warsaw, Indiana
FEI Number: 1825034
Product Type: Devices
Issue Date: November 09, 2023
Country: United States

Inspection History, 2009 to 2023

NAI1

VAI4

OAI2

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

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Biomet, Inc. FDA Form 483, Warsaw, Indiana, November 9, 2023