# Eurofins Ams Laboratories Pty Limited, Girraween, Australia – FDA Inspections

Source: https://www.keypedia.com/companies/eurofins-ams-laboratories-pty-limited/74537d96-5f56-4d70-894c-6869cae9677d

> Inspection records and compliance data for Eurofins Ams Laboratories Pty Limited in Girraween. 4 FDA inspections on record, 1 Form 483, last inspected November 04, 2022.

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## Details

- Name: Eurofins Ams Laboratories Pty Limited
- FEI Number: 3006635869
- Business Operations: API/FDF ANALYTICAL TESTING
- Address Line 1: 179 Magowar Rd
- City: Girraween
- Country Name: Australia
- Address: 179 Magowar Rd, Girraween, Australia
- Country: Australia

## Related Documents

- FDA Inspection 1191865 - Eurofins Ams Laboratories Pty Limited - 2022-11-04 — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2022
- FDA Inspection 1191865 - Eurofins Ams Laboratories Pty Limited - 2022-11-04 — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2022
- [FDA Inspection 1008506 - Eurofins Ams Laboratories Pty Limited - 2017-03-24](https://www.keypedia.com/records/fda_inspections/eurofins-ams-laboratories-pty-limited/785cc809-c079-4718-9f66-4dba23aa6f21) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2017
- FDA Inspection 1008506 - Eurofins Ams Laboratories Pty Limited - 2017-03-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2017
- FDA Inspection 845397 - Eurofins Ams Laboratories Pty Limited - 2013-07-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 24, 2013
- FDA Inspection 845397 - Eurofins Ams Laboratories Pty Limited - 2013-07-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 24, 2013
- FDA Inspection 653654 - Eurofins Ams Laboratories Pty Limited - 2010-03-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 3, 2010
- FDA Inspection 653654 - Eurofins Ams Laboratories Pty Limited - 2010-03-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 3, 2010

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