# Swissport USA Inc - Inspection Records

Source: https://www.keypedia.com/companies/swissport-usa-inc/8202b769-930f-4ecc-ac7c-ac22d1454b8f

> Inspection records and compliance data for Swissport USA Inc in Jamaica, New York. Access full analysis and detailed observations.

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## Details

- Name: Swissport USA Inc
- FEI Number: 3003279045
- City: Jamaica
- State: New York
- Country Name: United States
- Address Line 1: Jfk Int'L Airport Building 151  Room 300
- Zip Code: 11430

## Related Documents

- [483 - Swissport USA Inc - 2025-11-05](https://www.keypedia.com/records/483/swissport-usa-inc/32002608-8bef-484c-b7e2-bb5a5f74211f) — source: FDA, date: November 5, 2025
- [FDA Inspection 1291912 - Swissport USA Inc - 2025-11-05](https://www.keypedia.com/records/fda_inspections/swissport-usa-inc/17702cd7-fb47-40a0-8fe8-01cbdf69e3e3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 5, 2025
- [FDA Inspection 1236387 - Swissport USA Inc - 2024-04-17](https://www.keypedia.com/records/fda_inspections/swissport-usa-inc/a31fc5aa-92ea-417d-babb-78865ee55a45) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 17, 2024
- [FDA Inspection 1016318 - Swissport USA Inc - 2017-05-30](https://www.keypedia.com/records/fda_inspections/swissport-usa-inc/04425ab7-9a15-40af-b457-a60cf1dad53c) — classification: No Action Indicated (NAI), source: FDA, date: May 30, 2017
- [FDA Inspection 923211 - Swissport USA Inc - 2015-04-14](https://www.keypedia.com/records/fda_inspections/swissport-usa-inc/899a71cc-fa61-4edc-a12a-1153395937f4) — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2015
- [FDA Inspection 807592 - Swissport USA Inc - 2012-11-16](https://www.keypedia.com/records/fda_inspections/swissport-usa-inc/b3ce3df5-e33b-496a-a061-055f6b02fade) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2012
- [FDA Inspection 661325 - Swissport USA Inc - 2010-05-21](https://www.keypedia.com/records/fda_inspections/swissport-usa-inc/6190db01-e3a5-4605-964a-732774f59b92) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 21, 2010

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