# Radlink Inc - Inspection Records

Source: https://www.keypedia.com/companies/radlink-inc/ccf047eb-a16e-4080-afad-d0fae26db26f

> Inspection records and compliance data for Radlink Inc in El Segundo, California. Access full analysis and detailed observations.

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## Details

- Name: Radlink Inc
- FEI Number: 3005560996
- City: El Segundo
- State: California
- Country Name: United States
- Address Line 1: 2101 E El Segundo Blvd, ste 104
- Zip Code: 90245

## Related Documents

- [FDA Inspection 1050340 - Radlink Inc - 2018-02-07](https://www.keypedia.com/records/fda_inspections/radlink-inc/6e43f616-7317-4c39-97fd-be197526f3be) — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2018
- [FDA Inspection 1050340 - Radlink Inc - 2018-02-07](https://www.keypedia.com/records/fda_inspections/radlink-inc/84a1263f-c97e-44fb-9afc-61e85d56ef9b) — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2018
- [FDA Inspection 867734 - Radlink Inc - 2014-02-26](https://www.keypedia.com/records/fda_inspections/radlink-inc/385e2960-2259-44f0-a573-5d007ed9974b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 26, 2014
- [FDA Inspection 679348 - Radlink Inc - 2010-09-03](https://www.keypedia.com/records/fda_inspections/radlink-inc/0bcb46f4-36ad-436c-80f8-bf6305105023) — classification: No Action Indicated (NAI), source: FDA, date: September 3, 2010
- [FDA Inspection 679348 - Radlink Inc - 2010-09-03](https://www.keypedia.com/records/fda_inspections/radlink-inc/b45d4083-7d91-484b-bb28-e6597b78a630) — classification: No Action Indicated (NAI), source: FDA, date: September 3, 2010
- [FDA Inspection 562096 - Radlink Inc - 2009-01-26](https://www.keypedia.com/records/fda_inspections/radlink-inc/21e818b0-1ae1-49d8-a86e-458ac2a91a77) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 26, 2009
- [FDA Inspection 562096 - Radlink Inc - 2009-01-26](https://www.keypedia.com/records/fda_inspections/radlink-inc/e647fdfa-34bd-4a20-8fd7-915cbd4ee013) — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2009

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