# Delta Air Lines Inc. (NYSE: DAL), Louisville, KY – FDA Inspections

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

> Inspection records and compliance data for Delta Air Lines Inc. in Louisville, Kentucky. 7 FDA inspections on record, last inspected August 29, 2023. Publicly traded as NYSE: DAL.

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## Details

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

## Stock

- Stock ticker: DAL
- Exchange: NYSE
- Share price: $85.55
- Market cap: $56.3B
- Price as of: November 6, 2026

## Related Documents

- FDA Inspection 1216832 - Delta Air Lines Inc. - 2023-08-29 — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2023
- FDA Inspection 1216832 - Delta Air Lines Inc. - 2023-08-29 — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2023
- FDA Inspection 1085351 - Delta Air Lines Inc. - 2019-03-04 — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2019
- FDA Inspection 1019988 - Delta Air Lines Inc. - 2017-07-05 — classification: No Action Indicated (NAI), source: FDA, date: July 5, 2017
- FDA Inspection 1019989 - Delta Air Lines Inc. - 2017-07-05 — classification: No Action Indicated (NAI), source: FDA, date: July 5, 2017
- [FDA Inspection 978396 - Delta Air Lines Inc. - 2016-06-07](https://www.keypedia.com/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.keypedia.com/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 — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2009

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