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FDA Inspection
•Eurofins Amatsi Analytics•November 3, 2023

Eurofins Amatsi Analytics – FDA Inspection, Nov 3, 2023

Record Details

This FDA Inspection record concerns Eurofins Amatsi Analytics, with an inspection on November 3, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Eurofins Amatsi Analytics
Inspection Date
November 3, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Yiying E. Chen (Issuing Officer)
View Company Profile

ID · aed3d852-5c11-41b6-a617-8bef1b4eb2c9

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1224183
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

Other FDA inspections of Eurofins Amatsi Analytics

4
DateClassificationOfficeProject area
August 5, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 28, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 4, 2014NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
October 8, 2010NAICenter for Veterinary MedicinePre-Approval Eval. of Animal Drugs and Food Additives
Other documents for Eurofins Amatsi Analytics
  • FDA Inspection 1174252 - 2021-08-05
  • FDA Inspection 990192 - 2016-09-28
  • FDA Inspection 865532 - 2014-02-04
  • FDA Inspection 706532 - 2010-10-08

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