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FDA Inspection
•Otsuka Pharmaceutical Co. Ltd.•December 8, 2017

Otsuka Pharmaceutical Co. Ltd. – FDA Inspection, Dec 8, 2017

Record Details

This FDA Inspection record concerns Otsuka Pharmaceutical Co. Ltd., with an inspection on December 8, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Otsuka Pharmaceutical Co. Ltd.
Inspection Date
December 8, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Jose E. Melendez (FDA Associated Person)
View Company Profile

ID · 5a95822b-1dd5-488c-906a-0e6b80100cae

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1037241
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Otsuka Pharmaceutical Co. Ltd.

5
DateClassificationOfficeProject area
May 16, 2025NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 10, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 15, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 18, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 2, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Otsuka Pharmaceutical Co. Ltd.
  • FDA Inspection 1274284 - 2025-05-16
  • FDA Inspection 1112200 - 2019-10-10
  • FDA Inspection 969641 - 2016-04-15
  • FDA Inspection 899637 - 2014-09-18
  • FDA Inspection 796785 - 2012-08-02

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