FDA issued a Warning Letter to Teleflex Medical on 3/11/2014 for a previous inspection.
483 Teleflex Medical May 2014

483 Teleflex Medical May 2014

Patricia Mcilroy FDA$119.00 - Available Now

FDA investigators audited the Teleflex Medical - Arlington Heights, IL, United States facility and issued inspectional observations (via FDA 483) on 28 May 2014.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 28 May 2014
  • Location: Arlington Heights, United States
  • FEI: 1417411
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