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FDA Inspection
•Eurofins CDMO Alphora Inc.•December 2, 2011

FDA Inspection 757080 - Eurofins CDMO Alphora Inc. - December 02, 2011

Record Details

This FDA Inspection record concerns Eurofins CDMO Alphora Inc., with an inspection on December 2, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Eurofins CDMO Alphora Inc.
Inspection Date
December 2, 2011
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 6a59c591-5459-4e78-93ad-bb9714b6b918

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
757080
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Eurofins CDMO Alphora Inc.

4
DateClassificationOfficeProject area
January 17, 2025Not classifiedOffice of Inspections and Investigations
October 11, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 29, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 20, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Eurofins CDMO Alphora Inc.
  • FDA Inspection 1258608 - 2025-01-17
  • FDA Inspection 1106349 - 2019-10-11
  • FDA Inspection 972749 - 2016-04-29
  • FDA Inspection 870592 - 2014-02-20

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