FDA issued a Warning Letter to Cipla Limited on 2/25/2020 for a later inspection.
483 Cipla May 2013

483 Cipla May 2013

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FDA investigators audited the Cipla - Vasco Da Gama, India facility and issued inspectional observations (via FDA 483) on 30 May 2013.

Product details

  • Category: Human Drugs
  • Inspection end: 30 May 2013
  • Location: Vasco Da Gama, India
  • FEI: 3004081307
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