483 Daiichi Sankyo Sep 2014

483 Daiichi Sankyo Sep 2014

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FDA investigators audited the Daiichi Sankyo - Edison, NJ, United States facility and issued inspectional observations (via FDA 483) on 09 Sep 2014.

Product details

  • Category: Human Drugs
  • Inspection end: 09 Sep 2014
  • Location: Edison, United States
  • FEI: 3003089536
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