Gansu Heshui Longyuan Chinese Herbs Development Co, Ltd
FDA import alert and refusal historyXian, ChinaFEI 3005268338
As of October 26, 2026, Gansu Heshui Longyuan Chinese Herbs Development Co, Ltd (Xian, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for green tea extract powder, published by FDA on September 16, 2009, 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 Gansu Heshui Longyuan Chinese Herbs Development Co, Ltd
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listGreen Tea Extract PowderSource
Questions about Gansu Heshui Longyuan Chinese Herbs Development Co, Ltd
- Is Gansu Heshui Longyuan Chinese Herbs Development Co, Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Gansu Heshui Longyuan Chinese Herbs Development Co, Ltd is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for green tea extract powder; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Gansu Heshui Longyuan Chinese Herbs Development Co, Ltd?
- No FDA import refusals for Gansu Heshui Longyuan Chinese Herbs Development Co, Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Gansu Heshui Longyuan Chinese Herbs Development Co, Ltd's FEI number?
- Gansu Heshui Longyuan Chinese Herbs Development Co, Ltd's FDA Establishment Identifier (FEI) is 3005268338.
- Can shipments from Gansu Heshui Longyuan Chinese Herbs Development Co, Ltd still enter the U.S.?
- Shipments of green tea extract powder from Gansu Heshui Longyuan Chinese Herbs Development 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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