FDA Inspection 789805 — Sybaritic, Inc

Sybaritic, Inc — FEI 2131125

The FDA completed an inspection of Sybaritic, Inc on Jun 29, 2012 in Bloomington, MN. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Jun 29, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Bloomington, MN (United States)

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