FDA Inspection 1024590 — Livedo Usa, Inc.

Livedo Usa, Inc. — FEI 3004780365

The FDA completed an inspection of Livedo Usa, Inc. on July 19, 2017 in Wilson, NC. 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 19, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Wilson, NC (United States)