FDA issued a Warning Letter to Cordis Corporation on 7/7/2004 for a later inspection.
483 Cordis Dec 2003

483 Cordis Dec 2003

Jean Blackston Hill FDA, Stephanie Durso FDA, Jean Kelahan FDA, Kinh Mac FDA$119.00 - Available Now

FDA investigators audited the Cordis - Fremont, CA, United States facility and issued inspectional observations (via FDA 483) on 04 Dec 2003.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 04 Dec 2003
  • Location: Fremont, United States
  • FEI: 3000175337
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