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483 Response Hikma Pharmaceuticals USA, Jun 2005

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FDA investigators audited the Hikma Pharmaceuticals USA - Eatontown , NJ, United States facility and issued inspectional observation (via FDA 483) on 30 Jun 2005.

Product Details

  • Inspection end: 30 Jun 2005
  • Location: Eatontown, United States
  • FEI: 2250102
Hikma Pharmaceuticals USA FDA inspection 483 Jun 2005

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