# Delta Air Lines Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/delta-air-lines-inc/6c31232b-12d4-4b42-a7a5-6366a9b84b7c

> Inspection records and compliance data for Delta Air Lines Inc. in Louisville, Kentucky. Access full analysis and detailed observations.

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## Details

- Name: Delta Air Lines Inc.
- FEI Number: 1040044
- City: Louisville
- State: Kentucky
- Country Name: United States
- Address Line 1: 600 Terminal Dr Ste 4
- Zip Code: 40209

## Related Documents

- [FDA Inspection 1216832 - Delta Air Lines Inc. - 2023-08-29](https://www.globalkeysolutions.net/records/fda_inspections/delta-air-lines-inc/58bc5bf2-c767-4454-a3f6-a0a5af24a19f) — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2023
- [FDA Inspection 1216832 - Delta Air Lines Inc. - 2023-08-29](https://www.globalkeysolutions.net/records/fda_inspections/delta-air-lines-inc/ff873226-0f3f-4e22-b565-d4da6b738ebc) — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2023
- [FDA Inspection 1019989 - Delta Air Lines Inc. - 2017-07-05](https://www.globalkeysolutions.net/records/fda_inspections/delta-air-lines-inc/93cbe265-cc48-46c9-acda-65bbf62b35f0) — classification: No Action Indicated (NAI), source: FDA, date: July 5, 2017
- [FDA Inspection 978396 - Delta Air Lines Inc. - 2016-06-07](https://www.globalkeysolutions.net/records/fda_inspections/delta-air-lines-inc/3b67269e-5e4e-4d55-bb42-f563ccb57f5a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 7, 2016
- [FDA Inspection 800958 - Delta Air Lines Inc. - 2012-09-21](https://www.globalkeysolutions.net/records/fda_inspections/delta-air-lines-inc/9f7cbe04-6d2a-4ffc-a9f9-8e66f724388e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 21, 2012
- [FDA Inspection 578475 - Delta Air Lines Inc. - 2009-04-16](https://www.globalkeysolutions.net/records/fda_inspections/delta-air-lines-inc/7a189862-0027-4832-8372-59210f65ce10) — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2009

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