Miyama Cho Nogyo Kyodo Kumiai
FDA import alert and refusal historyMiyama-Cho, JapanFEI 11152
As of October 26, 2026, Miyama Cho Nogyo Kyodo Kumiai (Miyama-Cho, Japan) is on the red list of FDA Import Alert 99-36 (Low-acid canned/acidified foods: process information) for kyo-banboo (seasoned bamboo-sprout); vegetables (prepared) yamazatozuke; kitayama buki (seasoned colts-foots), 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 Miyama Cho Nogyo Kyodo Kumiai
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-36red listKyo-banboo (seasoned bamboo-sprout); vegetables (prepared) yamazatozuke; kitayama buki (seasoned colts-foots)Source
Questions about Miyama Cho Nogyo Kyodo Kumiai
- Is Miyama Cho Nogyo Kyodo Kumiai on an FDA import alert?
- Yes. As of October 26, 2026, Miyama Cho Nogyo Kyodo Kumiai is on the red list of FDA Import Alert 99-36, “Low-acid canned/acidified foods: process information”, for kyo-banboo (seasoned bamboo-sprout); vegetables (prepared) yamazatozuke; kitayama buki (seasoned colts-foots); FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Miyama Cho Nogyo Kyodo Kumiai?
- No FDA import refusals for Miyama Cho Nogyo Kyodo Kumiai appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Miyama Cho Nogyo Kyodo Kumiai's FEI number?
- Miyama Cho Nogyo Kyodo Kumiai's FDA Establishment Identifier (FEI) is 11152.
- Can shipments from Miyama Cho Nogyo Kyodo Kumiai still enter the U.S.?
- Shipments of kyo-banboo (seasoned bamboo-sprout); vegetables (prepared) yamazatozuke; kitayama buki (seasoned colts-foots) from Miyama Cho Nogyo Kyodo Kumiai 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).
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