Suzuki Shokai Co., Ltd.
FDA import alert and refusal historyNagoya, JapanFEI 3003204273
As of October 26, 2026, Suzuki Shokai Co., Ltd. (Nagoya, Japan) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for egg plant (fruit used as vegetable), ntrl/artfcl dried; egg plant (fruit used as vegetable), packaged food (not commercially sterile), 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 Suzuki Shokai 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 listEgg Plant (Fruit Used as Vegetable), Ntrl/Artfcl Dried; Egg Plant (Fruit Used as Vegetable), Packaged Food (Not Commercially Sterile)Source
Questions about Suzuki Shokai Co., Ltd.
- Is Suzuki Shokai Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Suzuki Shokai Co., Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for egg plant (fruit used as vegetable), ntrl/artfcl dried; egg plant (fruit used as vegetable), packaged food (not commercially sterile); FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Suzuki Shokai Co., Ltd.?
- No FDA import refusals for Suzuki Shokai Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Suzuki Shokai Co., Ltd.'s FEI number?
- Suzuki Shokai Co., Ltd.'s FDA Establishment Identifier (FEI) is 3003204273.
- Can shipments from Suzuki Shokai Co., Ltd. still enter the U.S.?
- Shipments of egg plant (fruit used as vegetable), ntrl/artfcl dried; egg plant (fruit used as vegetable), packaged food (not commercially sterile) from Suzuki Shokai 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).
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