Nanhai Yili Native Products Factory
FDA import alert and refusal historyFoshan, ChinaFEI 3012040886
Recorded by FDA as NANHAI YILI NATIVE PRODUCTS FACTORY
As of October 27, 2026, Nanhai Yili Native Products Factory (Foshan, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for dried fructus lycii; (aka goji berry); dried jujube, published by FDA on February 19, 2016, 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 Nanhai Yili Native Products Factory
1 record, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 99-08red listDried Fructus Lycii; (aka Goji Berry); Dried JujubeSource
Questions about Nanhai Yili Native Products Factory
- Is Nanhai Yili Native Products Factory on an FDA import alert?
- Yes. As of October 27, 2026, Nanhai Yili Native Products Factory is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for dried fructus lycii; (aka goji berry); dried jujube; FDA published the listing on February 19, 2016.
- Has FDA refused shipments from Nanhai Yili Native Products Factory?
- No FDA import refusals for Nanhai Yili Native Products Factory appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Nanhai Yili Native Products Factory's FEI number?
- Nanhai Yili Native Products Factory's FDA Establishment Identifier (FEI) is 3012040886.
- Can shipments from Nanhai Yili Native Products Factory still enter the U.S.?
- Shipments of dried fructus lycii; (aka goji berry); dried jujube from Nanhai Yili Native 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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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.