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FDA Inspection 842801 — Sybaritic, Inc

Sybaritic, Inc — FEI 2131125

The FDA completed an inspection of Sybaritic, Inc on August 9, 2013 in Bloomington, MN. 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
August 9, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Bloomington, MN (United States)

Facility

Other inspections at this facility

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  • 1179596 (NAI Thu Sep 08 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1152434 (NAI Thu Sep 16 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1096300 (NAI Tue Jul 02 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1044931 (OAI Wed Mar 07 2018 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

  • Injunction (116) (Tue Jan 05 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources