FDA issued a Warning Letter to Amgen, Inc. on 5/9/2003 for a previous inspection.
483 Amgen Sep 2010

483 Amgen Sep 2010

Kimberley Hoefen FDA, Ginger Sykes FDA$119.00 - Available Now

FDA investigators audited the Amgen - Boulder, CO, United States facility and issued inspectional observations (via FDA 483) on 03 Sep 2010.

Product details

  • Category: Human Drugs
  • Inspection end: 03 Sep 2010
  • Location: Boulder, United States
  • FEI: 3003072024
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