Marutai Co Ltd
FDA import alert and refusal historyFukuoka, JapanFEI 3012844802
Recorded by FDA as MARUTAI CO LTD
As of October 26, 2026, Marutai Co Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on April 23, 2018, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Soup, n.e.c. · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Marutai Co Ltd
2 records, newest first. Each line links to the FDA page it came from.
2018
- Import refusalSource
Refused, 2 lines in one entry: Soup, n.e.c.; Noodles and noodle products, n.e.c.NO ENGLISHEntry UPS-8265106-9Show 2 linesHide lines
- Refused, Soup, n.e.c.NO ENGLISHEntry UPS-8265106-9Source
- Refused, Noodles and noodle products, n.e.c.NO ENGLISHEntry UPS-8265106-9Source
Refusal charges, in plain English
- NO ENGLISH2 refused lines
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 Marutai Co Ltd
- Is Marutai Co Ltd on an FDA import alert?
- No listing for Marutai 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 Marutai Co Ltd?
- Yes. FDA refused 2 shipment lines from Marutai Co Ltd on April 23, 2018. The most recent, on April 23, 2018, was soup, n.e.c., charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Marutai Co Ltd's shipments?
- The most frequent charge is NO ENGLISH (required label information not in english, 2 lines).
- What is Marutai Co Ltd's FEI number?
- Marutai Co Ltd's FDA Establishment Identifier (FEI) is 3012844802.
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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.