FDA Inspection
Miyoshi America, IncMiyoshi America, Inc – FDA Inspection, Feb 6, 2026
Record Details
This FDA Inspection record concerns Miyoshi America, Inc, with an inspection on February 6, 2026, issued by the New England District Office, covering human drugs.
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ID · ac1adf18-2faf-4a07-8280-d7e05f2e174a
Inspection Facts
- Inspection number
- 1306728
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Miyoshi America, Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| 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 |
| July 20, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Miyoshi America, Inc
- FDA Inspection 1198326 - 2023-01-13
- FDA Inspection 1144549 - 2021-05-25
- FDA Inspection 974319 - 2016-06-03
- FDA Inspection 950532 - 2015-11-17
- FDA Inspection 737348 - 2011-07-20
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