Ito Shokuhin Kaisha Ltd FDA Record
- Latest inspection NAI · Jun 23, 2023
- No warning letters matched by name
Ito Shokuhin Kaisha Ltd has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Ito Shokuhin Kaisha Ltd" is on file.
- Latest inspection
- Jun 23, 2023 · 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 | 1 | 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 |
|---|---|---|---|---|
| Jun 23, 2023 | Shizuoka, Japan | Food/Cosmetics | No Action Indicated (NAI) | 3012229471 |
- 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 3012229471 | Shizuoka, Japan | 1 | Jun 23, 2023 |
Ito Shokuhin Kaisha Ltd and the FDA: common questions
Has Ito Shokuhin Kaisha Ltd received an FDA warning letter?
No FDA warning letter addressed to the name "Ito Shokuhin Kaisha 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 Ito Shokuhin Kaisha Ltd received an FDA Form 483?
FDA has not published a Form 483 for "Ito Shokuhin Kaisha Ltd" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Ito Shokuhin Kaisha Ltd?
The most recent FDA inspection on file ended Jun 23, 2023 at Shizuoka, Japan and was classified NAI. FDA has 1 inspection of Ito Shokuhin Kaisha Ltd on file.
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