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FDA Inspection 760057 — Defibtech, LLC

Defibtech, LLC — FEI 3003521780

The FDA completed an inspection of Defibtech, LLC on December 21, 2011 in Guilford, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 21, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Guilford, CT (United States)

Facility

Other inspections at this facility

  • 1024269 (NAI Wed Aug 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 876495 (NAI Fri Apr 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 708589 (VAI Tue Feb 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 675878 (OAI Wed Aug 18 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources