FDA Inspection
Eurofins Ams Laboratories Pty LimitedEurofins Ams Laboratories Pty Limited – FDA Inspection, Mar 24, 2017
Record Details
This FDA Inspection record concerns Eurofins Ams Laboratories Pty Limited, with an inspection on March 24, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 785cc809-c079-4718-9f66-4dba23aa6f21
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1008506
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Eurofins Ams Laboratories Pty Limited
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 4, 2022 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 24, 2013 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| March 3, 2010 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
Other documents for Eurofins Ams Laboratories Pty Limited
- FDA Inspection 1191865 - 2022-11-04
- FDA Inspection 845397 - 2013-07-24
- FDA Inspection 653654 - 2010-03-03
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