Home / Inspections / 789805

FDA Inspection 789805 — Sybaritic, Inc

Sybaritic, Inc — FEI 2131125

The FDA completed an inspection of Sybaritic, Inc on June 29, 2012 in Bloomington, MN. 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
June 29, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Bloomington, MN (United States)

Facility

Other inspections at this facility

  • 1221747 (NAI Thu Oct 05 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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