Kobayashi Seika Co.,Ltd.
FDA import alert and refusal historyEdogawa, JapanFEI 3009453417
Recorded by FDA as KOBAYASHI SEIKA CO.,LTD.
As of October 26, 2026, Kobayashi Seika Co.,Ltd. (Edogawa, Japan) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for baked snack food, n.e.c., published by FDA on September 18, 2009, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kobayashi Seika Co.,Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listBaked Snack Food, N.E.C.Source
Questions about Kobayashi Seika Co.,Ltd.
- Is Kobayashi Seika Co.,Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Kobayashi Seika Co.,Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for baked snack food, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Kobayashi Seika Co.,Ltd.?
- No FDA import refusals for Kobayashi Seika Co.,Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kobayashi Seika Co.,Ltd.'s FEI number?
- Kobayashi Seika Co.,Ltd.'s FDA Establishment Identifier (FEI) is 3009453417.
- Can shipments from Kobayashi Seika Co.,Ltd. still enter the U.S.?
- Shipments of baked snack food, n.e.c. from Kobayashi Seika Co.,Ltd. can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
Buying from Kobayashi Seika Co.,Ltd.?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.