FDA Inspection 991196 — Sybaritic, Inc

Sybaritic, Inc — FEI 2131125

The FDA completed an inspection of Sybaritic, Inc on Sep 7, 2016 in Bloomington, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 7, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Bloomington, MN (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.