FDA issued a Warning Letter to Zimmer Biomet, Inc. on 8/24/2018 for a later inspection.
483 Zimmer Biomet Jun 2014

483 Zimmer Biomet Jun 2014

Amy Graf FDA, Thomas Peter FDA$119.00 - Available Now

FDA investigators audited the Zimmer Biomet - Warsaw, IN, United States facility and issued 2 inspectional observations (via FDA 483) on 30 Jun 2014.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 2
  • Inspection end: 30 Jun 2014
  • Location: Warsaw, United States
  • FEI: 1825034
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