FDA Inspection 1038643 — CLARITY DESIGN, INC.

CLARITY DESIGN, INC. — FEI 3011883032

The FDA completed an inspection of CLARITY DESIGN, INC. on Jan 9, 2018 in Poway, CA. 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
Jan 9, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Poway, CA (United States)