# Piedmont Airlines, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/piedmont-airlines-inc/8dd27b76-c0ce-4623-a7da-12712a3bc27a

> Inspection records and compliance data for Piedmont Airlines, Inc. in Greer, South Carolina. Access full analysis and detailed observations.

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## Details

- Name: Piedmont Airlines, Inc.
- FEI Number: 3004154768
- City: Greer
- State: South Carolina
- Country Name: United States
- Address Line 1: 500 Aviation Pkwy Ste 10
- Zip Code: 29651

## Related Documents

- [FDA Inspection 1316878 - Piedmont Airlines, Inc. - 2026-05-12](https://www.globalkeysolutions.net/records/fda_inspections/piedmont-airlines-inc/2c61cf90-01e1-468e-8f08-28fee2583f49) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 12, 2026
- [FDA Inspection 1316878 - Piedmont Airlines, Inc. - 2026-05-12](https://www.globalkeysolutions.net/records/fda_inspections/piedmont-airlines-inc/fd4c0166-1456-44ae-999a-eb989534b0aa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 12, 2026
- [FDA Inspection 1062471 - Piedmont Airlines, Inc. - 2018-07-24](https://www.globalkeysolutions.net/records/fda_inspections/piedmont-airlines-inc/cb08c00e-c6d0-4436-b4ae-826f4d1f9bb4) — classification: No Action Indicated (NAI), source: FDA, date: July 24, 2018
- [FDA Inspection 927529 - Piedmont Airlines, Inc. - 2015-05-12](https://www.globalkeysolutions.net/records/fda_inspections/piedmont-airlines-inc/50800f79-7e10-4bb7-8c37-20976370bd31) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 12, 2015
- [FDA Inspection 927529 - Piedmont Airlines, Inc. - 2015-05-12](https://www.globalkeysolutions.net/records/fda_inspections/piedmont-airlines-inc/b7aa4935-a8e1-4f1b-be0e-85be850b89b4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 12, 2015
- [FDA Inspection 801022 - Piedmont Airlines, Inc. - 2012-08-30](https://www.globalkeysolutions.net/records/fda_inspections/piedmont-airlines-inc/7cc017e4-ae80-48c4-8b8f-5343714bdb95) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2012

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