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FDA Inspection 747437 — Medela Inc

Medela Inc — FEI 1419937

The FDA completed an inspection of Medela Inc on August 9, 2011 in Mchenry, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 9, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: 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))
  • 696530 (OAI Mon Nov 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources