FDA Inspection 1298050 — Global Interconnect, Inc.

Global Interconnect, Inc. — FEI 3004920696

The FDA completed an inspection of Global Interconnect, Inc. on January 7, 2026 in Pocasset, MA. 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
January 7, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Pocasset, MA (United States)