FDA issued a Warning Letter to Lupin Limited on 5/7/2009 as a result of this inspection.
483 Lupin Nov 2008

483 Lupin Nov 2008

Michael Goga FDA, Parul Patel FDA$119.00 - Available Now

FDA investigators audited the Lupin - Mandideep, India facility and issued inspectional observations (via FDA 483) on 12 Nov 2008.

Product details

  • Category: Human Drugs
  • Inspection end: 12 Nov 2008
  • Location: Mandideep, India
  • FEI: 3002807511
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