# Intertek Testing Services Australia Pty Ltd - Inspection Records

Source: https://www.keypedia.com/companies/intertek-testing-services-australia-pty-ltd/fde1bc35-fdec-460f-906b-bbd915560bc7

> Inspection records and compliance data for Intertek Testing Services Australia Pty Ltd in West Footscray, None. Access full analysis and detailed observations.

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## Details

- Name: Intertek Testing Services Australia Pty Ltd
- FEI Number: 3007869649
- City: West Footscray
- State: None
- Country Name: Australia
- Address Line 1: Building 1, 19-23 Paramount Rd
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1226848 - Intertek Testing Services Australia Pty Ltd - 2023-11-03](https://www.keypedia.com/records/fda_inspections/intertek-testing-services-australia-pty-ltd/a4cabfa6-0dc8-44e4-89d9-8d034702ce67) — classification: No Action Indicated (NAI), source: FDA, date: November 3, 2023
- [FDA Inspection 1226848 - Intertek Testing Services Australia Pty Ltd - 2023-11-03](https://www.keypedia.com/records/fda_inspections/intertek-testing-services-australia-pty-ltd/b6546d19-a74f-42d3-88db-1926a14f2eda) — classification: No Action Indicated (NAI), source: FDA, date: November 3, 2023
- [FDA Inspection 993762 - Intertek Testing Services Australia Pty Ltd - 2016-11-03](https://www.keypedia.com/records/fda_inspections/intertek-testing-services-australia-pty-ltd/f9c8f89a-5d65-430f-94ac-a067460b6415) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 3, 2016
- [FDA Inspection 752255 - Intertek Testing Services Australia Pty Ltd - 2011-11-02](https://www.keypedia.com/records/fda_inspections/intertek-testing-services-australia-pty-ltd/d1a4f988-1068-4dc2-8272-b3c3f0b68865) — classification: No Action Indicated (NAI), source: FDA, date: November 2, 2011
- [FDA Inspection 623903 - Intertek Testing Services Australia Pty Ltd - 2009-10-28](https://www.keypedia.com/records/fda_inspections/intertek-testing-services-australia-pty-ltd/75ce96bb-0a5e-4a9d-9d14-7b98e440c0bb) — classification: Official Action Indicated (OAI), source: FDA, date: October 28, 2009

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