Kobayashi Shokuhin Co., Ltd
FDA import alert and refusal historyYamagata, JapanFEI 10373
As of October 26, 2026, Kobayashi Shokuhin Co., Ltd (Yamagata, Japan) is on the red list of FDA Import Alert 99-36 (Low-acid canned/acidified foods: process information) for japanese mushroom in water, published by FDA on June 3, 2014, 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 99-36 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kobayashi Shokuhin Co., Ltd
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-36red listJapanese mushroom in waterSource
Questions about Kobayashi Shokuhin Co., Ltd
- Is Kobayashi Shokuhin Co., Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Kobayashi Shokuhin Co., Ltd is on the red list of FDA Import Alert 99-36, “Low-acid canned/acidified foods: process information”, for japanese mushroom in water; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Kobayashi Shokuhin Co., Ltd?
- No FDA import refusals for Kobayashi Shokuhin Co., Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kobayashi Shokuhin Co., Ltd's FEI number?
- Kobayashi Shokuhin Co., Ltd's FDA Establishment Identifier (FEI) is 10373.
- Can shipments from Kobayashi Shokuhin Co., Ltd still enter the U.S.?
- Shipments of japanese mushroom in water from Kobayashi Shokuhin Co., Ltd can be detained without physical examination under Import Alert 99-36; 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 Shokuhin 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.