# National Railroad Passenger Corporation (Amtrak) - Inspection Records

Source: https://www.keypedia.com/companies/national-railroad-passenger-corporation-amtrak/33c44cd2-695a-49c4-bb58-b60e84c0da35

> Inspection records and compliance data for National Railroad Passenger Corporation (Amtrak) in Richmond, Virginia. Access full analysis and detailed observations.

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## Details

- Name: National Railroad Passenger Corporation (Amtrak)
- FEI Number: 1130052
- City: Richmond
- State: Virginia
- Country Name: United States
- Address Line 1: 7519 Staples Mill Rd
- Zip Code: 23228

## Related Documents

- [FDA Inspection 1313550 - National Railroad Passenger Corporation (Amtrak) - 2026-04-15](https://www.keypedia.com/records/fda_inspections/national-railroad-passenger-corporation-amtrak/1cba84ae-8421-492d-ba0b-6944fe8fa256) — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2026
- [FDA Inspection 1110136 - National Railroad Passenger Corporation (Amtrak) - 2019-08-29](https://www.keypedia.com/records/fda_inspections/national-railroad-passenger-corporation-amtrak/ced38979-0f3d-44f2-875a-159ac784c1b4) — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2019
- [FDA Inspection 892494 - National Railroad Passenger Corporation (Amtrak) - 2014-08-07](https://www.keypedia.com/records/fda_inspections/national-railroad-passenger-corporation-amtrak/45549989-adde-4d43-92e0-d97cccf203c4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 7, 2014
- [FDA Inspection 680112 - National Railroad Passenger Corporation (Amtrak) - 2010-09-14](https://www.keypedia.com/records/fda_inspections/national-railroad-passenger-corporation-amtrak/21af3c41-9a03-468a-8afc-c2a7d1d58699) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 14, 2010
- [FDA Inspection 586848 - National Railroad Passenger Corporation (Amtrak) - 2009-06-05](https://www.keypedia.com/records/fda_inspections/national-railroad-passenger-corporation-amtrak/bfa6c17e-ab7a-4771-8aba-e1fc6387744b) — classification: No Action Indicated (NAI), source: FDA, date: June 5, 2009

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