Lanzhou Lisi International Tradi
FDA import alert and refusal historyLanzhou, ChinaFEI 3012157135
Recorded by FDA as LANZHOU LISI INTERNATIONAL TRADI
As of October 26, 2026, Lanzhou Lisi International Tradi is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between June 28, 2018 and July 23, 2018, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Mushrooms and other fungi products, whole (button), n.e.c. · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Lanzhou Lisi International Tradi
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY3 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Lanzhou Lisi International Tradi
- Is Lanzhou Lisi International Tradi on an FDA import alert?
- No listing for Lanzhou Lisi International Tradi appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the China page.
- Has FDA refused shipments from Lanzhou Lisi International Tradi?
- Yes. FDA refused 3 shipment lines from Lanzhou Lisi International Tradi between June 28, 2018 and July 23, 2018. The most recent, on July 23, 2018, was mushrooms and other fungi products, whole (button), n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Lanzhou Lisi International Tradi's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 3 lines).
- What is Lanzhou Lisi International Tradi's FEI number?
- Lanzhou Lisi International Tradi's FDA Establishment Identifier (FEI) is 3012157135.
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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.