Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd
FDA import alert and refusal historyGuangzhou, ChinaFEI 3004341418
As of October 26, 2026, Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd (Guangzhou, China) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for lychee, published by FDA on February 2, 2010, 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 list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd
1 record, newest first. Each line links to the FDA page it came from.
2010
- Import alert listingListed on Import Alert 99-21red listLycheeSource
Questions about Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd
- Is Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for lychee; FDA published the listing on February 2, 2010.
- Has FDA refused shipments from Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd?
- No FDA import refusals for Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd's FEI number?
- Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd's FDA Establishment Identifier (FEI) is 3004341418.
- Can shipments from Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd still enter the U.S.?
- Shipments of lychee from Guangzhou Shunmin Fenglong Agricultural Products Co., Ltd 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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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.