FDA issued a Warning Letter to Zevex, Inc. on 9/27/2002 for a previous inspection.
483 Zevex (dba MOOG Medical Devices Group) Sep 2018

483 Zevex (dba MOOG Medical Devices Group) Sep 2018

James Montero FDA, Matthew Vernon FDA$119.00 - Available Now

FDA investigators audited the Zevex (dba MOOG Medical Devices Group) - Salt Lake City, UT, United States facility and issued inspectional observations (via FDA 483) on 17 Sep 2018.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 17 Sep 2018
  • Location: Salt Lake City, United States
  • FEI: 1000117172
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