FDA issued a Warning Letter to Med-Mizer, Inc. on 7/21/2014 as a result of this inspection.
483 Med-Mizer Mar 2014

483 Med-Mizer Mar 2014

Joseph Strelnik FDA$119.00 - Available Now

FDA investigators audited the Med-Mizer - Batesville, IN, United States facility and issued inspectional observations (via FDA 483) on 07 Mar 2014.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 07 Mar 2014
  • Location: Batesville, United States
  • FEI: 3004976058
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