FDA issued a Warning Letter to Huvepharma Inc on 6/13/2013 for a later inspection.
483 Huvepharma Sep 2009

483 Huvepharma Sep 2009

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FDA investigators audited the Huvepharma - Saint Louis, MO, United States facility and issued 3 inspectional observations (via FDA 483) on 10 Sep 2009.

Product details

  • Category: Animal Drugs & Feeds
  • Number of Observations: 3
  • Inspection end: 10 Sep 2009
  • Location: Saint Louis, United States
  • FEI: 1940172
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