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483 Huvepharma, Jun 2011

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FDA investigators audited the Huvepharma - Saint Louis , MO, United States facility and issued inspectional observation (via FDA 483) on 16 Jun 2011.

Product Details

  • Inspection end: 16 Jun 2011
  • Location: Saint Louis, United States
  • FEI: 1940172
Huvepharma FDA inspection 483 Jun 2011

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