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FDA Inspection
•Miyoshi America, Inc•May 25, 2021

Miyoshi America, Inc – FDA Inspection, May 25, 2021

Record Details

This FDA Inspection record concerns Miyoshi America, Inc, with an inspection on May 25, 2021, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Miyoshi America, Inc
Inspection Date
May 25, 2021
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 2a38b802-d721-4010-afa3-2e555ecdbfe0

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
1144549
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Miyoshi America, Inc

5
DateClassificationOfficeProject area
February 6, 2026Not classifiedNew England District Office
January 13, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 3, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 17, 2015NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
July 20, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Miyoshi America, Inc
  • FDA Inspection 1306728 - 2026-02-06
  • FDA Inspection 1198326 - 2023-01-13
  • FDA Inspection 974319 - 2016-06-03
  • FDA Inspection 950532 - 2015-11-17
  • FDA Inspection 737348 - 2011-07-20

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