FDA Inspection 1096300 — Sybaritic, Inc

Sybaritic, Inc — FEI 2131125

The FDA completed an inspection of Sybaritic, Inc on July 2, 2019 in Bloomington, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 2, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Bloomington, MN (United States)