Okabe Goshikihama Factory FDA Record
Okabe Goshikihama Factory has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Okabe Goshikihama Factory" is on file.
- Latest inspection
- Jul 26, 2016 · 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 | 2 | 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 |
|---|---|---|---|---|
| Jul 26, 2016 | Iyo-Shi, Japan | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3011288255 |
| Dec 10, 2009 | Iyo-Shi, Japan | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3011288255 |
- 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 3011288255 | Iyo-Shi, Japan | 2 | Jul 26, 2016 |
Okabe Goshikihama Factory and the FDA: common questions
Has Okabe Goshikihama Factory received an FDA warning letter?
No FDA warning letter addressed to the name "Okabe Goshikihama 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 Okabe Goshikihama Factory received an FDA Form 483?
FDA has not published a Form 483 for "Okabe Goshikihama Factory" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Okabe Goshikihama Factory?
The most recent FDA inspection on file ended Jul 26, 2016 at Iyo-Shi, Japan and was classified VAI. FDA has 2 inspections of Okabe Goshikihama Factory on file.
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