Zimmer, Inc.

Form 483

Warsaw, Indiana, United StatesFEI 1000220733Issued October 16, 2017

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 1000220733.

Observations8

Issue DateOctober 16, 2017

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Zimmer, Inc.
Location: Warsaw, Indiana, United States
FEI Number: 1000220733
Product Type: Devices
Issue Date: October 16, 2017
Country: United States

Inspection History, 2009 to 2022

NAI2

VAI3

OAI5

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

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Zimmer, Inc. FDA Form 483, Warsaw, Indiana, October 16, 2017