FDA issued a Warning Letter to Lupin Limited on 5/7/2009 for a previous inspection.
483 Lupin Dec 2018

483 Lupin Dec 2018

Christopher Keating FDA, June Page FDA, Unnee Ranjan FDA, Pratik Upadhyay FDA$119.00 - Available Now

FDA investigators audited the Lupin - Mandideep, India facility and issued inspectional observations (via FDA 483) on 04 Dec 2018.

Product details

  • Category: Human Drugs
  • Inspection end: 04 Dec 2018
  • Location: Mandideep, India
  • FEI: 3002807511
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