483 PDS Dec 2001

483 PDS Dec 2001

Matthew Henciak FDA$119.00 - Available Now

FDA investigators audited the PDS - Laurel, MD, United States facility and issued inspectional observations (via FDA 483) on 05 Dec 2001.

Product details

  • Category: Human Drugs
  • Inspection end: 05 Dec 2001
  • Location: Laurel, United States
  • FEI: 3003080243
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