Takara Shokuhin
FDA import alert and refusal historyShozu-Gun, JapanFEI 3009867165
Recorded by FDA as TAKARA SHOKUHIN
As of October 26, 2026, Takara Shokuhin is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on February 12, 2018, most often for no scheduled process filed (NO PROCESS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Saury · NO PROCESS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Takara Shokuhin
3 records, newest first. Each line links to the FDA page it came from.
2018
- Import refusalSource
Refused, 3 lines in one entry: SauryNO PROCESSEntry 221-6110110-4Show 3 linesHide lines
- Refused, SauryNO PROCESSEntry 221-6110110-4Source
- Refused, SauryNO PROCESSEntry 221-6110110-4Source
- Refused, SauryNO PROCESSEntry 221-6110110-4Source
Refusal charges, in plain English
- NO PROCESS3 refused lines
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
Questions about Takara Shokuhin
- Is Takara Shokuhin on an FDA import alert?
- No listing for Takara Shokuhin appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.
- Has FDA refused shipments from Takara Shokuhin?
- Yes. FDA refused 3 shipment lines from Takara Shokuhin on February 12, 2018. The most recent, on February 12, 2018, was saury, charged as NO PROCESS (no scheduled process filed).
- Why did FDA refuse Takara Shokuhin's shipments?
- The most frequent charge is NO PROCESS (no scheduled process filed, 3 lines).
- What is Takara Shokuhin's FEI number?
- Takara Shokuhin's FDA Establishment Identifier (FEI) is 3009867165.
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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.