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FDA Inspection 1025861 — Kimball Electronics - Indianapolis

Kimball Electronics - Indianapolis — FEI 3004598644

The FDA completed an inspection of Kimball Electronics - Indianapolis on September 13, 2017 in Indianapolis, IN. 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
September 13, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Indianapolis, IN (United States)

Facility

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  • 1000623 (VAI Thu Dec 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 947450 (OAI Fri Oct 16 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources