483 Kennametal Stellite L.P. Sep 2018

483 Kennametal Stellite L.P. Sep 2018

Suyang Qin FDA$119.00 - Available Now

FDA investigators audited the Kennametal Stellite L.P. - Goshen, IN, United States facility and issued inspectional observations (via FDA 483) on 26 Sep 2018.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 26 Sep 2018
  • Location: Goshen, United States
  • FEI: 3009539841
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