FDA Inspection 1180322 — Keter Canada, Inc.

Keter Canada, Inc. — FEI 3010508078

The FDA completed an inspection of Keter Canada, Inc. on September 23, 2022 in Milton. 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
September 23, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Milton (Canada)