Kanshii Oita Co. Ltd. FDA Record
Kanshii Oita Co. Ltd. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Kanshii Oita Co. Ltd." is on file.
- Latest inspection
- Sep 20, 2017 · VAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 1 | Nov 14, 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 |
|---|---|---|---|---|
| Sep 20, 2017 | Oita, Japan | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3013654109 |
- 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 3013654109 | Oita, Japan | 1 | Sep 20, 2017 |
Kanshii Oita Co. Ltd. and the FDA: common questions
Has Kanshii Oita Co. Ltd. received an FDA warning letter?
No FDA warning letter addressed to the name "Kanshii Oita 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 Kanshii Oita Co. Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Kanshii Oita Co. Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Kanshii Oita Co. Ltd.?
The most recent FDA inspection on file ended Sep 20, 2017 at Oita, Japan and was classified VAI. FDA has 1 inspection of Kanshii Oita Co. Ltd. on file.
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