FDA issued a Warning Letter to Nostrum Laboratories Inc on 4/27/2009 for a previous inspection.
483 Nostrum Labs Nov 2010

483 Nostrum Labs Nov 2010

Tara Greene FDA, Megan Kirk FDA, Cody Rickman FDA, Matthew Sleeter FDA$119.00 - Available Now

FDA investigators audited the Nostrum Labs - Kansas City, MO, United States facility and issued inspectional observations (via FDA 483) on 05 Nov 2010.

Product details

  • Category: Human Drugs
  • Inspection end: 05 Nov 2010
  • Location: Kansas City, United States
  • FEI: 1930436
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