483 Corflex Jan 2017

483 Corflex Jan 2017

Abby Pelletier FDA$119.00 - Available Now

FDA investigators audited the Corflex - Manchester, NH, United States facility and issued 3 inspectional observations (via FDA 483) on 04 Jan 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 3
  • Inspection end: 04 Jan 2017
  • Location: Manchester, United States
  • FEI: 1218997
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