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FDA Inspection
•Ajinomoto Company Inc.•May 29, 2009

Ajinomoto Company Inc. – FDA Inspection, May 29, 2009

Record Details

This FDA Inspection record concerns Ajinomoto Company Inc., with an inspection on May 29, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Ajinomoto Company Inc.
Inspection Date
May 29, 2009
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 204165f1-9f5e-441f-baec-fac95d1ee3aa

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
592985
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Ajinomoto Company Inc.

5
DateClassificationOfficeProject area
February 21, 2025Not classifiedOffice of Inspections and Investigations
November 8, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 22, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 13, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 13, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Ajinomoto Company Inc.
  • FDA Inspection 1261618 - 2025-02-21
  • FDA Inspection 1112437 - 2019-11-08
  • FDA Inspection 1038111 - 2017-09-22
  • FDA Inspection 917041 - 2015-03-13
  • FDA Inspection 798908 - 2012-09-13

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