483 Intertek USA Nov 2017

483 Intertek USA Nov 2017

Lakecha Lewis FDA, Mohsen Rajabi Abhari FDA$119.00 - Available Now

FDA investigators audited the Intertek USA - San Diego, CA, United States facility and issued inspectional observations (via FDA 483) on 09 Nov 2017.

Product details

  • Category: Human Drugs
  • Inspection end: 09 Nov 2017
  • Location: San Diego, United States
  • FEI: 3004461652
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