FDA Inspection 1228543 — Northwest Eye Design, LLC

Northwest Eye Design, LLC — FEI 3005290929

The FDA completed an inspection of Northwest Eye Design, LLC on February 2, 2024 in Kirkland, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 2, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Kirkland, WA (United States)

Citations

IDCFRDescription
2279521 CFR 801.20(a)Label to bear a unique device identifier
323721 CFR 820.72(b)Remedial action