Moi Truong Xanh Co., Ltd
FDA import alert and refusal historySon Tra District, VietnamFEI 3013708129
As of October 26, 2026, Moi Truong Xanh Co., Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines between July 10, 2018 and July 20, 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
- Mahi mahi · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Moi Truong Xanh Co., Ltd
7 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY7 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.
- LACKS FIRM2 refused lines
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
Questions about Moi Truong Xanh Co., Ltd
- Is Moi Truong Xanh Co., Ltd on an FDA import alert?
- No listing for Moi Truong Xanh Co., Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Vietnam page.
- Has FDA refused shipments from Moi Truong Xanh Co., Ltd?
- Yes. FDA refused 7 shipment lines from Moi Truong Xanh Co., Ltd between July 10, 2018 and July 20, 2018. The most recent, on July 20, 2018, was mahi mahi, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Moi Truong Xanh Co., Ltd's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 7 lines) and LACKS FIRM (manufacturer name and address missing, 2 lines).
- What is Moi Truong Xanh Co., Ltd's FEI number?
- Moi Truong Xanh Co., Ltd's FDA Establishment Identifier (FEI) is 3013708129.
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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.