483 Actavis Jul 2016

483 Actavis Jul 2016

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FDA investigators audited the Actavis - Edison, NJ, United States facility and issued inspectional observations (via FDA 483) on 07 Jul 2016.

Product details

  • Category: Human Drugs
  • Inspection end: 07 Jul 2016
  • Location: Edison, United States
  • FEI: 3009017204
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