FDA issued a Warning Letter to Entellus Medical on 4/6/2017 as a result of this inspection.
483 Entellus Medical Sep 2016

483 Entellus Medical Sep 2016

Scott Golladay FDA, Kellie Thommes FDA$119.00 - Available Now

FDA investigators audited the Entellus Medical - Plymouth, MN, United States facility and issued inspectional observations (via FDA 483) on 27 Sep 2016.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 27 Sep 2016
  • Location: Plymouth, United States
  • FEI: 3006345872
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