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FDA Inspection 584203 — Neomend Inc

Neomend Inc — FEI 3001237235

The FDA completed an inspection of Neomend Inc on May 14, 2009 in Irvine, CA. 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
May 14, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)

Facility

Other inspections at this facility

  • 1022919 (NAI Thu Aug 10 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 941850 (VAI Tue Sep 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 934069 (NAI Thu Jun 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 780229 (NAI Thu May 03 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 701965 (NAI Wed Dec 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources