Koikeya Co., Ltd.
FDA import alert and refusal historyItabashi, JapanFEI 3001078729
As of October 25, 2026, Koikeya Co., Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on June 27, 2019, 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
- Baked snack food, n.e.c. · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Koikeya Co., Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2019
- Import refusalSource
Refused, 2 lines in one entry: Baked snack food, n.e.c.NO ENGLISHEntry 349-1006847-6Show 2 linesHide lines
- Refused, Baked snack food, n.e.c.NO ENGLISHEntry 349-1006847-6Source
- Refused, Baked snack food, n.e.c.NO ENGLISHEntry 349-1006847-6Source
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 Koikeya Co., Ltd.
- Is Koikeya Co., Ltd. on an FDA import alert?
- No listing for Koikeya Co., Ltd. appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Japan page.
- Has FDA refused shipments from Koikeya Co., Ltd.?
- Yes. FDA refused 2 shipment lines from Koikeya Co., Ltd. on June 27, 2019. The most recent, on June 27, 2019, was baked snack food, n.e.c., charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Koikeya Co., Ltd.'s shipments?
- The most frequent charge is NO ENGLISH (required label information not in english, 2 lines).
- What is Koikeya Co., Ltd.'s FEI number?
- Koikeya Co., Ltd.'s FDA Establishment Identifier (FEI) is 3001078729.
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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.