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FDA Inspection 589572 — Gentherm Medical, LLC

Gentherm Medical, LLC — FEI 1516825

The FDA completed an inspection of Gentherm Medical, LLC on July 15, 2009 in Blue Ash, OH. 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
July 15, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Blue Ash, OH (United States)

Facility

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  • 1003116 (NAI Wed Jan 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 820605 (NAI Fri Mar 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 753901 (NAI Fri Nov 18 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources