# United Airlines - Inspection Records

Source: https://www.keypedia.com/companies/united-airlines/df7f5bd9-d2d0-4e0f-b9c1-d42910c35903

> Inspection records and compliance data for United Airlines in Los Angeles, California. Access full analysis and detailed observations.

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## Details

- Name: United Airlines
- FEI Number: 2040042
- City: Los Angeles
- State: California
- Country Name: United States
- Address Line 1: 700 World Way
- Zip Code: 90045

## Related Documents

- [FDA Inspection 1304586 - United Airlines - 2026-02-23](https://www.keypedia.com/records/fda_inspections/united-airlines/eabf02a3-f132-4a81-b626-b966ebcba18e) — source: FDA, date: February 23, 2026
- [FDA Inspection 1304586 - United Airlines - 2026-02-23](https://www.keypedia.com/records/fda_inspections/united-airlines/9e7cbaa8-098f-422d-947f-56ebb6b13afb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 23, 2026
- [FDA Inspection 1102312 - United Airlines - 2019-08-21](https://www.keypedia.com/records/fda_inspections/united-airlines/53a26c1a-85ae-459e-8e9e-6210c1639ca4) — classification: No Action Indicated (NAI), source: FDA, date: August 21, 2019
- [FDA Inspection 1009756 - United Airlines - 2017-05-04](https://www.keypedia.com/records/fda_inspections/united-airlines/672aa7b1-498f-4e05-aec7-43cecdf33b9d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 4, 2017
- [FDA Inspection 856065 - United Airlines - 2013-11-21](https://www.keypedia.com/records/fda_inspections/united-airlines/556b9c5c-f3d2-497a-ae8c-2ba8ae343bea) — classification: No Action Indicated (NAI), source: FDA, date: November 21, 2013
- [FDA Inspection 743509 - United Airlines - 2011-09-08](https://www.keypedia.com/records/fda_inspections/united-airlines/c5b16de8-3c03-4ba2-9c14-81426d629b80) — classification: No Action Indicated (NAI), source: FDA, date: September 8, 2011
- [FDA Inspection 563185 - United Airlines - 2009-02-19](https://www.keypedia.com/records/fda_inspections/united-airlines/58a54fc6-8911-4f7e-874c-8ba5db8fd735) — classification: No Action Indicated (NAI), source: FDA, date: February 19, 2009

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