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FDA Inspection 761055 — Life Recovery Systems HD, LLC

Life Recovery Systems HD, LLC — FEI 3006059109

The FDA completed an inspection of Life Recovery Systems HD, LLC on January 4, 2012 in Kinnelon, NJ. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
January 4, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Kinnelon, NJ (United States)

Facility

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  • 969065 (NAI Mon Mar 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 794489 (NAI Tue Aug 14 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources