483 Southwest Technologies Mar 2019

483 Southwest Technologies Mar 2019

Eric Fox FDA$119.00 - Available Now

FDA investigators audited the Southwest Technologies - Kansas City, MO, United States facility and issued inspectional observations (via FDA 483) on 20 Mar 2019.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 20 Mar 2019
  • Location: Kansas City, United States
  • FEI: 1929833
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