FDA Inspection 729519 — Lowell, Inc.

Lowell, Inc. — FEI 3002462840

The FDA completed an inspection of Lowell, Inc. on Jun 8, 2011 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
Jun 8, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Brooklyn Park, MN (United States)