FDA issued a Warning Letter to Abbott (St Jude Medical Inc.) on 4/12/2017 for a previous inspection.
483 Abbott Aug 2019

483 Abbott Aug 2019

Nicole Gillette FDA, Leonard Lavi FDA$119.00 - Available Now

FDA investigators audited the Abbott - Sylmar, CA, United States facility and issued inspectional observations (via FDA 483) on 02 Aug 2019.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 02 Aug 2019
  • Location: Sylmar, United States
  • FEI: 2017865
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