Rumi Japan (Morimatsu Suisan Reita Co., Ltd.) FDA Record
- Latest inspection NAI · Feb 10, 2015
- No warning letters matched by name
Rumi Japan (Morimatsu Suisan Reita Co., Ltd.) has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Rumi Japan (Morimatsu Suisan Reita Co., Ltd.)" is on file.
- Latest inspection
- Feb 10, 2015 · NAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 11, 2026 (checked Nov 15, 2026, unchanged) | File dated Nov 10, 2026 | Current |
| 510(k) clearances | 0 | Nov 15, 2026 | File dated Nov 9, 2026 | Current |
| Inspections | 2 | Nov 15, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Feb 10, 2015 | Imabari, Japan | Food/Cosmetics | No Action Indicated (NAI) | 3004298298 |
| Nov 27, 2009 | Imabari, Japan | Food/Cosmetics | Official Action Indicated (OAI) | 3004298298 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3004298298 | Imabari, Japan | 2 | Feb 10, 2015 |
Rumi Japan (Morimatsu Suisan Reita Co., Ltd.) and the FDA: common questions
Has Rumi Japan (Morimatsu Suisan Reita Co., Ltd.) received an FDA warning letter?
No FDA warning letter addressed to the name "Rumi Japan (Morimatsu Suisan Reita Co., Ltd.)" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has Rumi Japan (Morimatsu Suisan Reita Co., Ltd.) received an FDA Form 483?
FDA has not published a Form 483 for "Rumi Japan (Morimatsu Suisan Reita Co., Ltd.)" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Rumi Japan (Morimatsu Suisan Reita Co., Ltd.)?
The most recent FDA inspection on file ended Feb 10, 2015 at Imabari, Japan and was classified NAI. FDA has 2 inspections of Rumi Japan (Morimatsu Suisan Reita Co., Ltd.) on file, 1 of them classified OAI (official action indicated).
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