FDA Inspection 1118871 — Vesta Inc.

Vesta Inc. — FEI 2182291

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

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