Biomet, Inc.

Form 483

Warsaw, Indiana, United StatesFEI 1825034Issued January 17, 2017

View Form 483 PDF

Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1825034.

Observations7

Issue DateJanuary 17, 2017

StatusNo Warning Letter

Establishment TypeMedical Device Manufacturer

Related Inspections7

Establishment Details

Firm: Biomet, Inc.
Location: Warsaw, Indiana, United States
FEI Number: 1825034
Establishment Type: Medical Device Manufacturer
Product Type: Devices
Issue Date: January 17, 2017
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.

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Biomet, Inc. FDA Form 483, Warsaw, Indiana, January 17, 2017