Tianjin Rimei International Trade Co. Ltd.
FDA import alert and refusal historyTanggu District, ChinaFEI 3004675128
As of October 26, 2026, Tianjin Rimei International Trade Co. Ltd. (Tanggu District, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for ginseng (herbal & botanical teas); ginseng (herbal & botanicals, not teas), 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 Tianjin Rimei International Trade 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 listGinseng (Herbal & Botanical Teas); Ginseng (Herbal & Botanicals, not Teas)Source
Questions about Tianjin Rimei International Trade Co. Ltd.
- Is Tianjin Rimei International Trade Co. Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Tianjin Rimei International Trade Co. Ltd. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for ginseng (herbal & botanical teas); ginseng (herbal & botanicals, not teas); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Tianjin Rimei International Trade Co. Ltd.?
- No FDA import refusals for Tianjin Rimei International Trade Co. Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Tianjin Rimei International Trade Co. Ltd.'s FEI number?
- Tianjin Rimei International Trade Co. Ltd.'s FDA Establishment Identifier (FEI) is 3004675128.
- Can shipments from Tianjin Rimei International Trade Co. Ltd. still enter the U.S.?
- Shipments of ginseng (herbal & botanical teas); ginseng (herbal & botanicals, not teas) from Tianjin Rimei International Trade 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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