483 Teleflex Medical Sep 2017

483 Teleflex Medical Sep 2017

Justine Corson FDA$119.00 - Available Now

FDA investigators audited the Teleflex Medical - Mansfield, MA, United States facility and issued inspectional observations (via FDA 483) on 20 Sep 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 20 Sep 2017
  • Location: Mansfield, United States
  • FEI: 1221601
Add To Cart