FDA Inspection
Miyoshi America, IncMiyoshi America, Inc – FDA Inspection, Jul 20, 2011
Record Details
This FDA Inspection record concerns Miyoshi America, Inc, with an inspection on July 20, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Miyoshi America, Inc
- Inspection Date
- July 20, 2011
- Product Type
- Drugs
View Company Profile
ID · 37d58ace-8951-4ef2-bb00-594b95adbcbc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 737348
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Miyoshi America, Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| February 6, 2026 | Not classified | New England District Office | |
| January 13, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 25, 2021 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 3, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 17, 2015 | NAI | Center for Food Safety and Applied Nutrition | Colors and Cosmetics Technology |
Other documents for Miyoshi America, Inc
- FDA Inspection 1306728 - 2026-02-06
- FDA Inspection 1198326 - 2023-01-13
- FDA Inspection 1144549 - 2021-05-25
- FDA Inspection 974319 - 2016-06-03
- FDA Inspection 950532 - 2015-11-17
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