483 Mitsubishi Tanabe Pharma Factory Sep 2017

483 Mitsubishi Tanabe Pharma Factory Sep 2017

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FDA investigators audited the Mitsubishi Tanabe Pharma Factory - San'yoonoda, Japan facility and issued inspectional observations (via FDA 483) on 22 Sep 2017.

Product details

  • Category: Human Drugs
  • Inspection end: 22 Sep 2017
  • Location: San'yoonoda, Japan
  • FEI: 3002808316
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