FDA issued a Warning Letter to Globalemed, LLC on 11/16/2005 as a result of this inspection.
483 Globalemed Jun 2005

483 Globalemed Jun 2005

Amber Chung FDA, Lori Lawless FDA, Theresa Smedley FDA$119.00 - Available Now

FDA investigators audited the Globalemed - Alexandria, VA, United States facility and issued inspectional observations (via FDA 483) on 17 Jun 2005.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 17 Jun 2005
  • Location: Alexandria, United States
  • FEI: 3002522587
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