483 Robert Clifford Dec 2017

483 Robert Clifford Dec 2017

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FDA investigators audited the Robert Clifford - Charleston, SC, United States facility and issued inspectional observations (via FDA 483) on 04 Dec 2017.

Product details

  • Category: Human Drugs
  • Inspection end: 04 Dec 2017
  • Location: Charleston, United States
  • FEI: 3013905462
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