FDA issued a Warning Letter to Gyrus ENT, LLC on 11/13/2006 for a previous inspection.
483 Gyrus ACMI Sep 2013

483 Gyrus ACMI Sep 2013

Daniel Aisen FDA$119.00 - Available Now

FDA investigators audited the Gyrus ACMI - Bartlett, TN, United States facility and issued 4 inspectional observations (via FDA 483) on 18 Sep 2013.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 4
  • Inspection end: 18 Sep 2013
  • Location: Bartlett, United States
  • FEI: 1037007
Add To Cart