483 Teva Parenteral Manufacturing Aug 2019

483 Teva Parenteral Manufacturing Aug 2019

Alan Kurtzberg FDA, Linda Murphy FDA$119.00 - Available Now

FDA investigators audited the Teva Parenteral Manufacturing - Irvine, CA, United States facility and issued inspectional observations (via FDA 483) on 30 Aug 2019.

Product details

  • Category: Human Drugs
  • Inspection end: 30 Aug 2019
  • Location: Irvine, United States
  • FEI: 2027158
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