FDA Inspection 1118871 — Vesta Inc.

Vesta Inc. — FEI 2182291

The FDA completed an inspection of Vesta Inc. on January 31, 2020 in Franklin, WI. 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
January 31, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Franklin, WI (United States)