# Exeltis USA, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/exeltis-usa-inc/d5a2dfa6-39bc-4768-b3f4-5c0630d2dc8f

> Inspection records and compliance data for Exeltis USA, Inc. in Florham Park, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: Exeltis USA, Inc.
- FEI Number: 3008163531
- City: Florham Park
- State: New Jersey
- Country Name: United States
- Address Line 1: 180 Park Ave Ste 101
- Zip Code: 07932

## Related Documents

- [FDA Inspection 1250586 - Exeltis USA, Inc. - 2025-07-02](https://www.keypedia.com/records/fda_inspections/exeltis-usa-inc/675c00a3-94f3-4fb5-b4c0-26375be77d4b) — source: FDA, date: July 2, 2025
- [FDA Inspection 1250586 - Exeltis USA, Inc. - 2025-07-02](https://www.keypedia.com/records/fda_inspections/exeltis-usa-inc/a35bcf11-1032-4fdb-af70-333e22692648) — classification: No Action Indicated (NAI), source: FDA, date: July 2, 2025
- [FDA Inspection 1232731 - Exeltis USA, Inc. - 2024-11-15](https://www.keypedia.com/records/fda_inspections/exeltis-usa-inc/90fe4972-d279-4bf5-8705-4913c115dc11) — source: FDA, date: November 15, 2024
- [FDA Inspection 1232731 - Exeltis USA, Inc. - 2024-11-15](https://www.keypedia.com/records/fda_inspections/exeltis-usa-inc/b86074bd-b3c8-4819-9049-13279bf8a78d) — classification: No Action Indicated (NAI), source: FDA, date: November 15, 2024
- [FDA Inspection 1014140 - Exeltis USA, Inc. - 2017-06-06](https://www.keypedia.com/records/fda_inspections/exeltis-usa-inc/906d22db-852b-481c-80ce-fbc019fe6546) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 6, 2017
- [FDA Inspection 1014140 - Exeltis USA, Inc. - 2017-06-06](https://www.keypedia.com/records/fda_inspections/exeltis-usa-inc/9ab7c541-da1d-41e2-8960-4fde32f2506c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 6, 2017
- [FDA Inspection 1014140 - Exeltis USA, Inc. - 2017-06-06](https://www.keypedia.com/records/fda_inspections/exeltis-usa-inc/52efe546-6d6c-41bc-b1ba-f9be9697867e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 6, 2017

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