FDA issued a Warning Letter to CORPAK MedSystems, Inc. on 4/10/2013 for a previous inspection.
483 CORPAK MedSystems Mar 2014

483 CORPAK MedSystems Mar 2014

Raul Alicea FDA, Jesse Vazquez FDA$119.00 - Available Now

FDA investigators audited the CORPAK MedSystems - Buffalo Grove, IL, United States facility and issued 4 inspectional observations (via FDA 483) on 07 Mar 2014.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 4
  • Inspection end: 07 Mar 2014
  • Location: Buffalo Grove, United States
  • FEI: 1419949
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