FDA issued a Warning Letter to CORPAK MedSystems, Inc. on 4/10/2013 as a result of this inspection.
483 CORPAK MedSystems Jan 2013

483 CORPAK MedSystems Jan 2013

Andrew Leboeuf FDA$119.00 - Available Now

FDA investigators audited the CORPAK MedSystems - Buffalo Grove, IL, United States facility and issued inspectional observations (via FDA 483) on 04 Jan 2013.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 04 Jan 2013
  • Location: Buffalo Grove, United States
  • FEI: 1419949
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