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483 Huvepharma, Sep 2009

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by Kathleen Swat FDA

FDA investigators audited the Huvepharma - Saint Louis , MO, United States facility and issued inspectional observation (via FDA 483) on 10 Sep 2009.

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Product Details

  • Inspection end: 10 Sep 2009
  • Location: Saint Louis, United States
  • FEI: 1940172
Huvepharma FDA inspection 483 Sep 2009

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