FDA Inspection 1208179 — Shent USA, Inc.

Shent USA, Inc. — FEI 1222168

The FDA completed an inspection of Shent USA, Inc. on June 9, 2023 in Northborough, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 9, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Northborough, MA (United States)