483 Sanofi-Aventis Deutschland Mar 2017

483 Sanofi-Aventis Deutschland Mar 2017

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FDA investigators audited the Sanofi-Aventis Deutschland - Frankfurt am Main, Germany facility and issued inspectional observations (via FDA 483) on 03 Mar 2017.

Product details

  • Category: Human Drugs
  • Inspection end: 03 Mar 2017
  • Location: Frankfurt am Main, Germany
  • FEI: 3003195501
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