South Project China Herb Factory
FDA import alert and refusal historyShenzhen, ChinaFEI 3000817032
As of October 26, 2026, South Project China Herb Factory (Shenzhen, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for red panax ginseng, published by FDA on September 16, 2009, is also listed on Import Alert 99-19 (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 99-08 · red listIA 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for South Project China Herb Factory
2 records, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listmixed herbs other than teasSource
- Import alert listingListed on Import Alert 99-08red listRed Panax GinsengSource
Questions about South Project China Herb Factory
- Is South Project China Herb Factory on an FDA import alert?
- Yes. As of October 26, 2026, South Project China Herb Factory is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for red panax ginseng; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from South Project China Herb Factory?
- No FDA import refusals for South Project China Herb Factory appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is South Project China Herb Factory's FEI number?
- South Project China Herb Factory's FDA Establishment Identifier (FEI) is 3000817032.
- Can shipments from South Project China Herb Factory still enter the U.S.?
- Shipments of red panax ginseng from South Project China Herb 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.