Yamamasa Co., Ltd.
FDA import alert and refusal historyUji, JapanFEI 3000301750
As of October 26, 2026, Yamamasa Co., Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 10, 2025, most often for net quantity statement missing (LACKS N/C).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Tea, n.e.c. · LACKS N/C
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Yamamasa Co., Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Tea, n.e.c.LACKS N/CNO ENGLISHEntry 799-7952335-5Source
Refusal charges, in plain English
- LACKS N/C1 refused line
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- NO ENGLISH1 refused line
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
Questions about Yamamasa Co., Ltd.
- Is Yamamasa Co., Ltd. on an FDA import alert?
- No listing for Yamamasa Co., Ltd. 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 Yamamasa Co., Ltd.?
- Yes. FDA refused 1 shipment line from Yamamasa Co., Ltd. on June 10, 2025. The most recent, on June 10, 2025, was tea, n.e.c., charged as LACKS N/C (net quantity statement missing).
- Why did FDA refuse Yamamasa Co., Ltd.'s shipments?
- The most frequent charges are LACKS N/C (net quantity statement missing, 1 line) and NO ENGLISH (required label information not in english, 1 line).
- What is Yamamasa Co., Ltd.'s FEI number?
- Yamamasa Co., Ltd.'s FDA Establishment Identifier (FEI) is 3000301750.
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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.