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483 Paolo DePetrillo, MD, Feb 2018

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FDA investigators audited the Paolo DePetrillo, MD - Baltimore , MD, United States facility and issued inspectional observations (via FDA 483) on 28 Feb 2018.

Product Details

  • Category: Human Drugs
  • Inspection end: 28 Feb 2018
  • Location: Baltimore, United States
  • FEI: 3014064351
Paolo DePetrillo, MD FDA inspection 483 Feb 2018