# Intertek USA Inc. - Inspection Records

Source: https://www.keypedia.com/companies/intertek-usa-inc/2c61102d-28cb-4e8b-b5c0-01d3148f07d0

> Inspection records and compliance data for Intertek USA Inc. in Whitehouse, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: Intertek USA Inc.
- FEI Number: 1000151295
- City: Whitehouse
- State: New Jersey
- Country Name: United States
- Address Line 1: 291 Route 22 East
- Zip Code: 08888
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1286506 - Intertek USA Inc. - 2025-09-25](https://www.keypedia.com/records/fda_inspections/intertek-usa-inc/031da5d1-ce6e-4e03-bd74-a8e33707b93d) — source: FDA, date: September 25, 2025
- [FDA Inspection 1286506 - Intertek USA Inc. - 2025-09-25](https://www.keypedia.com/records/fda_inspections/intertek-usa-inc/7f342edb-ce60-471e-9a19-d9c6d57e4047) — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2025
- [483 - Intertek USA Inc. - 2025-03-07](https://www.keypedia.com/records/483/intertek-usa-inc/f6d61ea3-e37e-4c8f-baf6-9fa58b8576f8) — source: FDA, date: March 7, 2025
- [FDA Inspection 1263062 - Intertek USA Inc. - 2025-03-07](https://www.keypedia.com/records/fda_inspections/intertek-usa-inc/e6965e1f-e11f-479a-9c29-88858d51ae2b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 7, 2025
- [FDA Inspection 1135115 - Intertek USA Inc. - 2020-12-21](https://www.keypedia.com/records/fda_inspections/intertek-usa-inc/2f48af36-ffc7-461e-9310-010d26e42ceb) — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2020
- [FDA Inspection 981650 - Intertek USA Inc. - 2016-08-12](https://www.keypedia.com/records/fda_inspections/intertek-usa-inc/55df2482-54f0-4339-9b35-8ddf9cc459fb) — classification: No Action Indicated (NAI), source: FDA, date: August 12, 2016
- [FDA Inspection 815726 - Intertek USA Inc. - 2013-01-21](https://www.keypedia.com/records/fda_inspections/intertek-usa-inc/e7a3457b-9987-41b5-8ccb-28b5d0db710b) — classification: No Action Indicated (NAI), source: FDA, date: January 21, 2013
- [FDA Inspection 647477 - Intertek USA Inc. - 2010-03-03](https://www.keypedia.com/records/fda_inspections/intertek-usa-inc/0d58826a-4b3a-4030-91f5-a3b87b4613e1) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2010

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## Related Officers

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