FDA issued a Warning Letter to Abbott (St Jude Medical Inc.) on 4/12/2017 for a later inspection.
483 St Jude Medical Jul 2009

483 St Jude Medical Jul 2009

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FDA investigators audited the St Jude Medical - Sylmar, CA, United States facility and issued inspectional observations (via FDA 483) on 08 Jul 2009.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 08 Jul 2009
  • Location: Sylmar, United States
  • FEI: 2017865
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