Research Center of Ginseng and Medicinal Materials
FDA import alert and refusal historyHo Chi Minh City, VietnamFEI 3005715901
As of October 26, 2026, Research Center of Ginseng and Medicinal Materials (Ho Chi Minh City, Vietnam) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for ginseng tablets; pastilles, 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 Research Center of Ginseng and Medicinal Materials
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listGinseng tablets; pastillesSource
Questions about Research Center of Ginseng and Medicinal Materials
- Is Research Center of Ginseng and Medicinal Materials on an FDA import alert?
- Yes. As of October 26, 2026, Research Center of Ginseng and Medicinal Materials is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for ginseng tablets; pastilles; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Research Center of Ginseng and Medicinal Materials?
- No FDA import refusals for Research Center of Ginseng and Medicinal Materials appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Research Center of Ginseng and Medicinal Materials's FEI number?
- Research Center of Ginseng and Medicinal Materials's FDA Establishment Identifier (FEI) is 3005715901.
- Can shipments from Research Center of Ginseng and Medicinal Materials still enter the U.S.?
- Shipments of ginseng tablets; pastilles from Research Center of Ginseng and Medicinal Materials 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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