Goodwave Technology Development Limited
FDA import alert and refusal historyHaikoushi, ChinaFEI 3009319046
As of October 25, 2026, Goodwave Technology Development Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between July 19, 2019 and December 10, 2019, 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
- Ginger root (root & tuber vegetable) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Goodwave Technology Development Limited
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 Goodwave Technology Development Limited
- Is Goodwave Technology Development Limited on an FDA import alert?
- No listing for Goodwave Technology Development Limited appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the China page.
- Has FDA refused shipments from Goodwave Technology Development Limited?
- Yes. FDA refused 3 shipment lines from Goodwave Technology Development Limited between July 19, 2019 and December 10, 2019. The most recent, on December 10, 2019, was ginger root (root & tuber vegetable), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Goodwave Technology Development Limited's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 3 lines).
- What is Goodwave Technology Development Limited's FEI number?
- Goodwave Technology Development Limited's FDA Establishment Identifier (FEI) is 3009319046.
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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.