Weifang Gourmet Art and Craft Co., Ltd
FDA import alert and refusal historyShandong, ChinaFEI 3007178539
As of October 26, 2026, Weifang Gourmet Art and Craft Co., Ltd (Shandong, China) is on the red list of FDA Import Alert 99-31 (Food products: melamine and melamine analogs) for chocolate/cocoa products/cocoa beans; gelatin/rennet/pudding mixes/pie fillings, 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 Weifang Gourmet Art and Craft Co., Ltd
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-31red listChocolate/Cocoa Products/Cocoa beans; Gelatin/Rennet/Pudding Mixes/Pie FillingsSource
Questions about Weifang Gourmet Art and Craft Co., Ltd
- Is Weifang Gourmet Art and Craft Co., Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Weifang Gourmet Art and Craft Co., Ltd is on the red list of FDA Import Alert 99-31, “Food products: melamine and melamine analogs”, for chocolate/cocoa products/cocoa beans; gelatin/rennet/pudding mixes/pie fillings; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Weifang Gourmet Art and Craft Co., Ltd?
- No FDA import refusals for Weifang Gourmet Art and Craft Co., Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Weifang Gourmet Art and Craft Co., Ltd's FEI number?
- Weifang Gourmet Art and Craft Co., Ltd's FDA Establishment Identifier (FEI) is 3007178539.
- Can shipments from Weifang Gourmet Art and Craft Co., Ltd still enter the U.S.?
- Shipments of chocolate/cocoa products/cocoa beans; gelatin/rennet/pudding mixes/pie fillings from Weifang Gourmet Art and Craft Co., Ltd 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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