FDA Inspection
Miyoshi America, IncMiyoshi America, Inc – FDA Inspection, Jan 13, 2023
Record Details
This FDA Inspection record concerns Miyoshi America, Inc, with an inspection on January 13, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.
View Company Profile
ID · 3da6d54d-300a-4547-9433-a29e7c20d217
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1198326
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Miyoshi America, Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| February 6, 2026 | Not classified | New England District Office | |
| 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 1306728 - 2026-02-06
- FDA Inspection 1144549 - 2021-05-25
- FDA Inspection 974319 - 2016-06-03
- FDA Inspection 950532 - 2015-11-17
- FDA Inspection 737348 - 2011-07-20
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.