Kyokuyo Shokuhin Co., Ltd Shiogama Factory
FDA import alert and refusal historyShiogama, JapanFEI 3009863890
As of October 27, 2026, Kyokuyo Shokuhin Co., Ltd Shiogama Factory is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 12, 2025, most often for food additive unsafe under section 409 (UNSAFE ADD).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Crab, imitation · UNSAFE ADD
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Kyokuyo Shokuhin Co., Ltd Shiogama Factory
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Crab, imitationUNSAFE ADDEntry 442-4445140-5Source
2024
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Refusal charges, in plain English
- UNSAFE ADD1 refused line
Food additive unsafe under section 409
The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.
Questions about Kyokuyo Shokuhin Co., Ltd Shiogama Factory
- Is Kyokuyo Shokuhin Co., Ltd Shiogama Factory on an FDA import alert?
- No listing for Kyokuyo Shokuhin Co., Ltd Shiogama Factory appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Japan page.
- Has FDA refused shipments from Kyokuyo Shokuhin Co., Ltd Shiogama Factory?
- Yes. FDA refused 1 shipment line from Kyokuyo Shokuhin Co., Ltd Shiogama Factory on June 12, 2025. The most recent, on June 12, 2025, was crab, imitation, charged as UNSAFE ADD (food additive unsafe under section 409).
- Why did FDA refuse Kyokuyo Shokuhin Co., Ltd Shiogama Factory's shipments?
- The most frequent charge is UNSAFE ADD (food additive unsafe under section 409, 1 line).
- When was Kyokuyo Shokuhin Co., Ltd Shiogama Factory last inspected by FDA?
- FDA's most recent inspection of Kyokuyo Shokuhin Co., Ltd Shiogama Factory with a final classification is dated February 27, 2024 and was classified VAI (Voluntary Action Indicated).
- What is Kyokuyo Shokuhin Co., Ltd Shiogama Factory's FEI number?
- Kyokuyo Shokuhin Co., Ltd Shiogama Factory's FDA Establishment Identifier (FEI) is 3009863890.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.