FDA issued a Warning Letter to Electro-Cap International, Inc. on 7/20/2011 for a previous inspection.
483 Electro Cap International Jan 2015

483 Electro Cap International Jan 2015

Teresa Kastner FDA, Philip Woodward FDA$119.00 - Available Now

FDA investigators audited the Electro Cap International - Eaton, OH, United States facility and issued 6 inspectional observations (via FDA 483) on 23 Jan 2015.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 6
  • Inspection end: 23 Jan 2015
  • Location: Eaton, United States
  • FEI: 1000119368
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