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483 Jubilant Pharmova, Dec 2018

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by Saleem Akhtar FDA, Zedong Dong FDA, Dipesh Shah FDA

FDA investigators audited the Jubilant Pharmova - Mysore, India facility and issued inspectional observation (via FDA 483) on 18 Dec 2018.

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Product Details

  • Inspection end: 18 Dec 2018
  • Location: Mysore, India
  • FEI: 3003144728
Jubilant Pharmova FDA inspection 483 Dec 2018

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