FDA Inspection 917726 — Lattice Inc

Lattice Inc — FEI 3009542936

The FDA completed an inspection of Lattice Inc on March 12, 2015 in Wheaton, 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
March 12, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Wheaton, IL (United States)