483 GTIMD Oct 2018

483 GTIMD Oct 2018

James Whitney FDA$119.00 - Available Now

FDA investigators audited the GTIMD - Amherst, NH, United States facility and issued inspectional observations (via FDA 483) on 17 Oct 2018.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 17 Oct 2018
  • Location: Amherst, United States
  • FEI: 3009432325
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