Zimmer, Inc.

Form 483

Warsaw, Indiana, United StatesFEI 1000220733Issued July 11, 2015

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 1000220733.

Observations12

Issue DateJuly 11, 2015

StatusNo Warning Letter

Establishment TypeMedical Device Manufacturer

Related Inspections10

Establishment Details

Firm: Zimmer, Inc.
Location: Warsaw, Indiana, United States
FEI Number: 1000220733
Establishment Type: Medical Device Manufacturer
Product Type: Devices
Issue Date: July 11, 2015
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, July 11, 2015