xi'an green-life natural products co.,ltd
FDA import alert and refusal historyXian, ChinaFEI 3006508016
As of October 26, 2026, xi'an green-life natural products co.,ltd (Xian, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for notoginseng extract; pseudoginseng extract; sanchi root powder, published by FDA on December 30, 2014, 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 xi'an green-life natural products co.,ltd
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-08red listNotoginseng extract; Pseudoginseng extract; Sanchi Root powderSource
Questions about xi'an green-life natural products co.,ltd
- Is xi'an green-life natural products co.,ltd on an FDA import alert?
- Yes. As of October 26, 2026, xi'an green-life natural products co.,ltd is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for notoginseng extract; pseudoginseng extract; sanchi root powder; FDA published the listing on December 30, 2014.
- Has FDA refused shipments from xi'an green-life natural products co.,ltd?
- No FDA import refusals for xi'an green-life natural products co.,ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is xi'an green-life natural products co.,ltd's FEI number?
- xi'an green-life natural products co.,ltd's FDA Establishment Identifier (FEI) is 3006508016.
- Can shipments from xi'an green-life natural products co.,ltd still enter the U.S.?
- Shipments of notoginseng extract; pseudoginseng extract; sanchi root powder from xi'an green-life natural products co.,ltd 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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