# Piedmont Airlines - Inspection Records

Source: https://www.keypedia.com/companies/piedmont-airlines/6faa0b00-d650-405a-b6d5-dd533cc5f431

> Inspection records and compliance data for Piedmont Airlines in Omaha, Nebraska. Access full analysis and detailed observations.

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## Details

- Name: Piedmont Airlines
- FEI Number: 3011361844
- City: Omaha
- State: Nebraska
- Country Name: United States
- Address Line 1: 4501 Abbott Dr
- Zip Code: 68110

## Related Documents

- [FDA Inspection 1265064 - Piedmont Airlines - 2025-03-18](https://www.keypedia.com/records/fda_inspections/piedmont-airlines/81231434-1590-4bab-a258-90c722f950fb) — source: FDA, date: March 18, 2025
- [FDA Inspection 1265064 - Piedmont Airlines - 2025-03-18](https://www.keypedia.com/records/fda_inspections/piedmont-airlines/34c8324f-a522-4832-bea7-2160a5651d14) — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2025
- [FDA Inspection 1265064 - Piedmont Airlines - 2025-03-18](https://www.keypedia.com/records/fda_inspections/piedmont-airlines/9d7914c0-761d-4dd1-ade0-682b29bbad1b) — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2025
- [FDA Inspection 1261783 - Piedmont Airlines - 2025-01-29](https://www.keypedia.com/records/fda_inspections/piedmont-airlines/34dd8c11-18da-4ff2-b7bb-af76a1e4dc43) — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2025
- [FDA Inspection 1095578 - Piedmont Airlines - 2019-05-14](https://www.keypedia.com/records/fda_inspections/piedmont-airlines/5d4dc7bb-1017-47ac-bfe4-356b6142e4aa) — classification: No Action Indicated (NAI), source: FDA, date: May 14, 2019
- [FDA Inspection 1053512 - Piedmont Airlines - 2018-05-21](https://www.keypedia.com/records/fda_inspections/piedmont-airlines/5e5b47f2-280d-4857-9aec-455da9f046a1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 21, 2018
- [FDA Inspection 947853 - Piedmont Airlines - 2015-08-26](https://www.keypedia.com/records/fda_inspections/piedmont-airlines/f3465fab-4754-4cca-b1a5-aaf753f02dfe) — classification: No Action Indicated (NAI), source: FDA, date: August 26, 2015

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