xuancheng baicao plants industry and trade co.,ltd
FDA import alert and refusal historyAnhui, ChinaFEI 3004683318
As of October 27, 2026, xuancheng baicao plants industry and trade co.,ltd (Anhui, China) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for super arthgold; pro arthmax, published by FDA on November 28, 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 54-16 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for xuancheng baicao plants industry and trade co.,ltd
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 54-16red listSuper ArthGold; Pro ArthMaxSource
Questions about xuancheng baicao plants industry and trade co.,ltd
- Is xuancheng baicao plants industry and trade co.,ltd on an FDA import alert?
- Yes. As of October 27, 2026, xuancheng baicao plants industry and trade co.,ltd is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for super arthgold; pro arthmax; FDA published the listing on November 28, 2014.
- Has FDA refused shipments from xuancheng baicao plants industry and trade co.,ltd?
- No FDA import refusals for xuancheng baicao plants industry and trade co.,ltd appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is xuancheng baicao plants industry and trade co.,ltd's FEI number?
- xuancheng baicao plants industry and trade co.,ltd's FDA Establishment Identifier (FEI) is 3004683318.
- Can shipments from xuancheng baicao plants industry and trade co.,ltd still enter the U.S.?
- Shipments of super arthgold; pro arthmax from xuancheng baicao plants industry and trade co.,ltd can be detained without physical examination under Import Alert 54-16; 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.