FDA Inspection 648102 — Sybaritic, Inc

Sybaritic, Inc — FEI 2131125

The FDA completed an inspection of Sybaritic, Inc on March 5, 2010 in Bloomington, MN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
March 5, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Bloomington, MN (United States)

Citations

IDCFRDescription
10005n/aProcedural requirements