FDA issued a Warning Letter to Covidien LP on 6/14/2012 as a result of this inspection.
483 Covidien, LP Feb 2012

483 Covidien, LP Feb 2012

Edward Janik FDA, Jeffrey Thibodeau FDA$119.00 - Available Now

FDA investigators audited the Covidien, LP - North Haven, CT, United States facility and issued inspectional observations (via FDA 483) on 09 Feb 2012.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 09 Feb 2012
  • Location: North Haven, United States
  • FEI: 1219930
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