Kaizouya
FDA import alert and refusal historyHyogo Pref, JapanFEI 14547
As of October 26, 2026, Kaizouya (Hyogo Pref, Japan) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for gourd, dried or paste, published by FDA on September 16, 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 99-21 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kaizouya
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-21red listGourd, Dried or PasteSource
Questions about Kaizouya
- Is Kaizouya on an FDA import alert?
- Yes. As of October 26, 2026, Kaizouya is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for gourd, dried or paste; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Kaizouya?
- No FDA import refusals for Kaizouya appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kaizouya's FEI number?
- Kaizouya's FDA Establishment Identifier (FEI) is 14547.
- Can shipments from Kaizouya still enter the U.S.?
- Shipments of gourd, dried or paste from Kaizouya can be detained without physical examination under Import Alert 99-21; 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 Kaizouya?
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.