FDA issued a Warning Letter to Shandong Vianor Biotech Co., Ltd. on 9/12/2017 as a result of this inspection.
483 Shandong Vianor Biotech May 2017

483 Shandong Vianor Biotech May 2017

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FDA investigators audited the Shandong Vianor Biotech - Linyi, China facility and issued inspectional observations (via FDA 483) on 10 May 2017.

Product details

  • Category: Human Drugs
  • Inspection end: 10 May 2017
  • Location: Linyi, China
  • FEI: 3011717652
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