FDA issued a Warning Letter to ITG-Medev Inc on 9/7/2018 as a result of this inspection.
483 ITG-Medev Jun 2018

483 ITG-Medev Jun 2018

Sara Richardson FDA$119.00 - Available Now

FDA investigators audited the ITG-Medev - San Francisco, CA, United States facility and issued inspectional observations (via FDA 483) on 06 Jun 2018.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 06 Jun 2018
  • Location: San Francisco, United States
  • FEI: 1000307251
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