FDA Inspection 1110192 — Fivos, Inc.

Fivos, Inc. — FEI 3008850288

The FDA completed an inspection of Fivos, Inc. on November 7, 2019 in West Lebanon, NH. 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
November 7, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
West Lebanon, NH (United States)