483 Arcamed Mar 2018

483 Arcamed Mar 2018

Debara Reese FDA$119.00 - Available Now

FDA investigators audited the Arcamed - Indianapolis, IN, United States facility and issued inspectional observations (via FDA 483) on 06 Mar 2018.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 06 Mar 2018
  • Location: Indianapolis, United States
  • FEI: 3010622588
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