Yikang Group Limited Company of Shandong
FDA import alert and refusal historyZaozhuang, ChinaFEI 3006397179
As of October 26, 2026, Yikang Group Limited Company of Shandong (Zaozhuang, China) is on the red list of FDA Import Alert 99-31 (Food products: melamine and melamine analogs) for bakery products/dough/mixes/icings; chocolate/cocoa products/cocoa beans, 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 99-31 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Yikang Group Limited Company of Shandong
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-31red listBakery Products/Dough/Mixes/Icings; Chocolate/Cocoa Products/Cocoa beansSource
Questions about Yikang Group Limited Company of Shandong
- Is Yikang Group Limited Company of Shandong on an FDA import alert?
- Yes. As of October 26, 2026, Yikang Group Limited Company of Shandong is on the red list of FDA Import Alert 99-31, “Food products: melamine and melamine analogs”, for bakery products/dough/mixes/icings; chocolate/cocoa products/cocoa beans; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Yikang Group Limited Company of Shandong?
- No FDA import refusals for Yikang Group Limited Company of Shandong appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Yikang Group Limited Company of Shandong's FEI number?
- Yikang Group Limited Company of Shandong's FDA Establishment Identifier (FEI) is 3006397179.
- Can shipments from Yikang Group Limited Company of Shandong still enter the U.S.?
- Shipments of bakery products/dough/mixes/icings; chocolate/cocoa products/cocoa beans from Yikang Group Limited Company of Shandong can be detained without physical examination under Import Alert 99-31; 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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