FDA issued a Warning Letter to Jubilant Generics Limited on 3/6/2019 for a later inspection.
483 Jubilant Generics Mar 2015

483 Jubilant Generics Mar 2015

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FDA investigators audited the Jubilant Generics - Sikanderpur Bhainswal, India facility and issued inspectional observations (via FDA 483) on 13 Mar 2015.

Product details

  • Category: Human Drugs
  • Inspection end: 13 Mar 2015
  • Location: Sikanderpur Bhainswal, India
  • FEI: 3006895982
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