FDA issued a Warning Letter to Teleflex Medical on 3/11/2014 as a result of this inspection.
483 Teleflex Medical Sep 2013

483 Teleflex Medical Sep 2013

Nicole Williams FDA$119.00 - Available Now

FDA investigators audited the Teleflex Medical - Arlington Heights, IL, United States facility and issued 5 inspectional observations (via FDA 483) on 24 Sep 2013.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 5
  • Inspection end: 24 Sep 2013
  • Location: Arlington Heights, United States
  • FEI: 1417411
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