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FDA Inspection 719276 — Hooper Holmes, Inc.

Hooper Holmes, Inc. — FEI 1000118383

The FDA completed an inspection of Hooper Holmes, Inc. on April 18, 2011 in Olathe, KS. 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
April 18, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Olathe, KS (United States)

Facility

Other inspections at this facility

  • 1019167 (NAI Wed Jul 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 821760 (VAI Thu Mar 07 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 730902 (VAI Fri Jun 17 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 670528 (OAI Wed Jun 23 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources