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FDA Inspection
•Ajinomoto Omnichem NV•October 5, 2016

Ajinomoto Omnichem NV – FDA Inspection, Oct 5, 2016

Record Details

This FDA Inspection record concerns Ajinomoto Omnichem NV, with an inspection on October 5, 2016, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Ajinomoto Omnichem NV
Inspection Date
October 5, 2016
Product Type
Veterinary
Office
Center for Veterinary Medicine
Person
  • Kellia N. Hicks (FDA Associated Person)
View Company Profile

ID · 3c916edb-4985-4cf1-a0df-502d2adc209b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
987961
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Outcome
Form 483 issued

Other FDA inspections of Ajinomoto Omnichem NV

4
DateClassificationOfficeProject area
March 16, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 22, 2018VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
January 24, 2014NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
December 4, 2009VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Ajinomoto Omnichem NV
  • FDA Inspection 1201241 - 2022-03-16
  • FDA Inspection 1057656 - 2018-06-22
  • FDA Inspection 865733 - 2014-01-24
  • FDA Inspection 637173 - 2009-12-04

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