FDA Inspection 994804 — Blueroot Health, Inc.

Blueroot Health, Inc. — FEI 3005564444

The FDA completed an inspection of Blueroot Health, Inc. on December 9, 2016 in Middletown, CT. 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
December 9, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Middletown, CT (United States)