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FDA Inspection
•Tomita Pharmaceutical Co., Ltd.•May 23, 2025

Tomita Pharmaceutical Co., Ltd. – FDA Inspection, May 23, 2025

Record Details

This FDA Inspection record concerns Tomita Pharmaceutical Co., Ltd., with an inspection on May 23, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Tomita Pharmaceutical Co., Ltd.
Inspection Date
May 23, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Lillian S. Wu (Issuing Officer)
View Company Profile

ID · 4f6013e3-b91f-4ff9-80dc-38c5b88386c8

Inspection Facts

Inspection number
1274910
FDA center
Human Drugs

Other FDA inspections of Tomita Pharmaceutical Co., Ltd.

7
DateClassificationOfficeProject area
November 8, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 9, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 29, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 1, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 1, 2013VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
View all 7 other inspections on the company page
Other documents for Tomita Pharmaceutical Co., Ltd.
  • FDA Inspection 1113539 - 2019-11-08
  • FDA Inspection 1045598 - 2018-03-09
  • FDA Inspection 981352 - 2016-07-29
  • FDA Inspection 860359 - 2013-11-01
  • FDA Inspection 860351 - 2013-11-01

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