FDA Inspection 1022388 — Maui Jim, Inc.

Maui Jim, Inc. — FEI 3002647555

The FDA completed an inspection of Maui Jim, Inc. on July 13, 2017 in Peoria, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 13, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Peoria, IL (United States)