Nozaki Tsukemono Co Ltd
FDA import alert and refusal historyMiyazaki, JapanFEI 1000339196
As of October 26, 2026, Nozaki Tsukemono Co Ltd (Miyazaki, Japan) is on the red list of FDA Import Alert 45-06 (Stevia leaves, crude extracts and foods containing them) for pickled radish/ amakuchi katsuo takuan yagurashibori konbu; salted radish; white radish (root & tuber vegetable), cultured/cured, 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 45-06 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Nozaki Tsukemono Co Ltd
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-06red listPickled Radish/ Amakuchi Katsuo Takuan Yagurashibori Konbu; salted radish; White Radish (Root & Tuber Vegetable), Cultured/CuredSource
Questions about Nozaki Tsukemono Co Ltd
- Is Nozaki Tsukemono Co Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Nozaki Tsukemono Co Ltd is on the red list of FDA Import Alert 45-06, “Stevia leaves, crude extracts and foods containing them”, for pickled radish/ amakuchi katsuo takuan yagurashibori konbu; salted radish; white radish (root & tuber vegetable), cultured/cured; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Nozaki Tsukemono Co Ltd?
- No FDA import refusals for Nozaki Tsukemono Co Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Nozaki Tsukemono Co Ltd's FEI number?
- Nozaki Tsukemono Co Ltd's FDA Establishment Identifier (FEI) is 1000339196.
- Can shipments from Nozaki Tsukemono Co Ltd still enter the U.S.?
- Shipments of pickled radish/ amakuchi katsuo takuan yagurashibori konbu; salted radish; white radish (root & tuber vegetable), cultured/cured from Nozaki Tsukemono Co Ltd can be detained without physical examination under Import Alert 45-06; 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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