Ajinomoto General Foods
FDA import alert and refusal historyShinjuku, JapanFEI 3013214294
Recorded by FDA as AJINOMOTO GENERAL FOODS
As of October 26, 2026, Ajinomoto General Foods is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between March 2, 2017 and March 8, 2017, 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
- Tea, green · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ajinomoto General Foods
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Tea, greenNO ENGLISHEntry UPS-2155536-3Source
- Import refusalRefused, Beverage base not mentioned elsewhere, n.e.c.NO ENGLISHEntry UPS-2153711-4Source
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 Ajinomoto General Foods
- Is Ajinomoto General Foods on an FDA import alert?
- No listing for Ajinomoto General Foods 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 Ajinomoto General Foods?
- Yes. FDA refused 2 shipment lines from Ajinomoto General Foods between March 2, 2017 and March 8, 2017. The most recent, on March 8, 2017, was tea, green, charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Ajinomoto General Foods's shipments?
- The most frequent charge is NO ENGLISH (required label information not in english, 2 lines).
- What is Ajinomoto General Foods's FEI number?
- Ajinomoto General Foods's FDA Establishment Identifier (FEI) is 3013214294.
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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.