FDA issued a Warning Letter to Zimmer Manufacturing B.V. on 9/19/2012 as a result of this inspection.
483 Zimmer Manufacturing B.V. Jun 2012

483 Zimmer Manufacturing B.V. Jun 2012

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FDA investigators audited the Zimmer Manufacturing B.V. - Mercedita, PR, United States facility and issued 2 inspectional observations (via FDA 483) on 22 Jun 2012.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 2
  • Inspection end: 22 Jun 2012
  • Location: Mercedita, United States
  • FEI: 1000132037
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