FDA issued a Warning Letter to NuVasive Inc on 3/12/2013 for a later inspection.
483 NuVasive Dec 2008

483 NuVasive Dec 2008

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FDA investigators audited the NuVasive - San Diego, CA, United States facility and issued inspectional observations (via FDA 483) on 02 Dec 2008.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 02 Dec 2008
  • Location: San Diego, United States
  • FEI: 3002980729
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