# FDA Inspection 1298050 - Global Interconnect, Inc. - January 07, 2026

Source: https://www.keypedia.com/records/fda_inspections/global-interconnect-inc/63f76b9c-155c-483c-9f0e-4b8e9bb9f30e
Source feed: FDA_Inspections

> FDA Inspection 1298050 for Global Interconnect, Inc. on January 07, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1298050
- Company Name: Global Interconnect, Inc.
- Inspection Date: 2026-01-07
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices

## Related Documents

- [FDA Inspection 1298050 - 2026-01-07](https://www.keypedia.com/records/fda_inspections/global-interconnect-inc/7bc610b2-489b-42df-8b4c-8bd8a954516c)
- [FDA Inspection 1298050 - 2026-01-07](https://www.keypedia.com/records/fda_inspections/global-interconnect-inc/0f52382b-7b3d-49cc-b0f0-c30eabd6b750)
- [FDA Inspection 1049924 - 2018-04-24](https://www.keypedia.com/records/fda_inspections/global-interconnect-inc/5667bd6c-895e-43c3-bd12-9f37cbccfdc9)

Company: https://www.keypedia.com/companies/global-interconnect-inc/1deb12b2-d953-47d6-a03a-87d1918c17b3