KUKI SANGYO CO., LTD. Takenari Factory FDA Record
- Latest inspection NAI · Aug 4, 2016
- No warning letters matched by name
KUKI SANGYO CO., LTD. Takenari Factory has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "KUKI SANGYO CO., LTD. Takenari Factory" is on file.
- Latest inspection
- Aug 4, 2016 · 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 |
Reviewing KUKI SANGYO CO., LTD. Takenari Factory as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or check KUKI SANGYO CO., LTD. Takenari Factory yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.
Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Aug 4, 2016 | Mie-Gun, Japan | Food/Cosmetics | No Action Indicated (NAI) | 3004666154 |
- 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 3004666154 | Mie-Gun, Japan | 1 | Aug 4, 2016 |
KUKI SANGYO CO., LTD. Takenari Factory and the FDA: common questions
Has KUKI SANGYO CO., LTD. Takenari Factory received an FDA warning letter?
No FDA warning letter addressed to the name "KUKI SANGYO CO., LTD. Takenari Factory" 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 KUKI SANGYO CO., LTD. Takenari Factory received an FDA Form 483?
FDA has not published a Form 483 for "KUKI SANGYO CO., LTD. Takenari Factory" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect KUKI SANGYO CO., LTD. Takenari Factory?
The most recent FDA inspection on file ended Aug 4, 2016 at Mie-Gun, Japan and was classified NAI. FDA has 1 inspection of KUKI SANGYO CO., LTD. Takenari Factory on file.
Need more than this page shows? Ask about KUKI SANGYO CO., LTD. Takenari Factory in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.