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FDA Inspection 696530 — Medela Inc

Medela Inc — FEI 1419937

The FDA completed an inspection of Medela Inc on November 1, 2010 in Mchenry, IL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 1, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mchenry, IL (United States)

Facility

Other inspections at this facility

  • 893426 (NAI Wed Aug 27 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 869654 (NAI Wed Feb 26 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 779907 (OAI Fri May 25 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 755250 (NAI Mon Nov 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 747437 (VAI Tue Aug 09 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources