FDA Inspection 1194244 — Lowell, Inc.

Lowell, Inc. — FEI 3002462840

The FDA completed an inspection of Lowell, Inc. on Dec 6, 2022 in Brooklyn Park, MN. 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
Dec 6, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Brooklyn Park, MN (United States)