FDA issued a Warning Letter to Nostrum Laboratories Inc on 4/27/2009 for a later inspection.
483 Nostrum Labs Aug 2001

483 Nostrum Labs Aug 2001

Cynthia Evitt FDA, Minerva Rogers 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 29 Aug 2001.

Product details

  • Category: Human Drugs
  • Inspection end: 29 Aug 2001
  • Location: Kansas City, United States
  • FEI: 1930436
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