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483 Huvepharma, May 2018

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by Kellia Hicks FDA

FDA investigators audited the Huvepharma - Saint Louis , MO, United States facility and issued inspectional observation (via FDA 483) on 22 May 2018.

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Product Details

  • Inspection end: 22 May 2018
  • Location: Saint Louis, United States
  • FEI: 1940172
Huvepharma FDA inspection 483 May 2018

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