Jiangmen Shuangshuang Rice Noodle Products Factory
FDA import alert and refusal historyJiang Men, ChinaFEI 3008360964
Recorded by FDA as JIANGMEN SHUANGSHUANG RICE NOODLE PRODUCTS FACTORY
As of October 27, 2026, Jiangmen Shuangshuang Rice Noodle Products Factory (Jiang Men, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for preserved beans with ginger, published by FDA on April 5, 2012, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Jiangmen Shuangshuang Rice Noodle Products Factory
1 record, newest first. Each line links to the FDA page it came from.
2012
- Import alert listingListed on Import Alert 99-08red listPreserved Beans With GingerSource
Questions about Jiangmen Shuangshuang Rice Noodle Products Factory
- Is Jiangmen Shuangshuang Rice Noodle Products Factory on an FDA import alert?
- Yes. As of October 27, 2026, Jiangmen Shuangshuang Rice Noodle Products Factory is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for preserved beans with ginger; FDA published the listing on April 5, 2012.
- Has FDA refused shipments from Jiangmen Shuangshuang Rice Noodle Products Factory?
- No FDA import refusals for Jiangmen Shuangshuang Rice Noodle Products Factory appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Jiangmen Shuangshuang Rice Noodle Products Factory's FEI number?
- Jiangmen Shuangshuang Rice Noodle Products Factory's FDA Establishment Identifier (FEI) is 3008360964.
- Can shipments from Jiangmen Shuangshuang Rice Noodle Products Factory still enter the U.S.?
- Shipments of preserved beans with ginger from Jiangmen Shuangshuang Rice Noodle Products Factory can be detained without physical examination under Import Alert 99-08; 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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