FDA Inspection 842801 — Sybaritic, Inc

Sybaritic, Inc — FEI 2131125

The FDA completed an inspection of Sybaritic, Inc on Aug 9, 2013 in Bloomington, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 9, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Bloomington, MN (United States)

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