483 Michael P. Whyte, MD Mar 2015

483 Michael P. Whyte, MD Mar 2015

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FDA investigators audited the Michael P. Whyte, MD - Saint Louis, MO, United States facility and issued inspectional observations (via FDA 483) on 11 Mar 2015.

Product details

  • Category: Human Drugs
  • Inspection end: 11 Mar 2015
  • Location: Saint Louis, United States
  • FEI: 3011343841
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