Liangcheng Shuguo Subsidiary Foodstuffs Factory
FDA import alert and refusal historyWenheng, ChinaFEI 3015217562
As of October 26, 2026, Liangcheng Shuguo Subsidiary Foodstuffs Factory (Wenheng, China) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for dried sweet potato, published by FDA on May 17, 2019, is also listed on Import Alert 99-22 (red list), 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 99-21 · red listIA 99-22 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Liangcheng Shuguo Subsidiary Foodstuffs Factory
2 records, newest first. Each line links to the FDA page it came from.
2019
- Import alert listingListed on Import Alert 99-21red listDried Sweet PotatoSource
- Import alert listingListed on Import Alert 99-22red listDried Sweet PotatoSource
Questions about Liangcheng Shuguo Subsidiary Foodstuffs Factory
- Is Liangcheng Shuguo Subsidiary Foodstuffs Factory on an FDA import alert?
- Yes. As of October 26, 2026, Liangcheng Shuguo Subsidiary Foodstuffs Factory is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for dried sweet potato; FDA published the listing on May 17, 2019.
- Has FDA refused shipments from Liangcheng Shuguo Subsidiary Foodstuffs Factory?
- No FDA import refusals for Liangcheng Shuguo Subsidiary Foodstuffs Factory appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Liangcheng Shuguo Subsidiary Foodstuffs Factory's FEI number?
- Liangcheng Shuguo Subsidiary Foodstuffs Factory's FDA Establishment Identifier (FEI) is 3015217562.
- Can shipments from Liangcheng Shuguo Subsidiary Foodstuffs Factory still enter the U.S.?
- Shipments of dried sweet potato from Liangcheng Shuguo Subsidiary Foodstuffs Factory can be detained without physical examination under Import Alert 99-21; 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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