FDA issued a Warning Letter to Zimmer Manufacturing B.V. on 9/19/2012 for a previous inspection.
483 Zimmer Manufacturing B.V. Nov 2015

483 Zimmer Manufacturing B.V. Nov 2015

Laiza Garcia FDA, Kimberly Lewandowski-Walker FDA, Adaliz Santaliz-Cruz FDA$119.00 - Available Now

FDA investigators audited the Zimmer Manufacturing B.V. - Mercedita, PR, United States facility and issued inspectional observation (via FDA 483) on 17 Nov 2015.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 17 Nov 2015
  • Location: Mercedita, United States
  • FEI: 1000132037
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