AboutBlogOver 40,000+ FDA inspection documents: 483s, EIRs, 483Rs

483 Intas Pharmaceuticals, Nov 2009

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FDA investigators audited the Intas Pharmaceuticals - Ahmedabad, India facility and issued inspectional observations (via FDA 483) on 13 Nov 2009.

Product Details

  • Category: Human Drugs
  • Inspection end: 13 Nov 2009
  • Location: Ahmedabad, India
  • FEI: 3003157498
Intas Pharmaceuticals FDA inspection 483 Nov 2009

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