Guangzhou Qingxintang Zhiyao Coltd
FDA import alert and refusal historyGuangzhou, ChinaFEI 3014127563
Recorded by FDA as GUANGZHOU QINGXINTANG ZHIYAO COLTD
As of October 26, 2026, Guangzhou Qingxintang Zhiyao Coltd is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between November 10, 2020 and December 28, 2020, 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
- Dates, dried or paste · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Guangzhou Qingxintang Zhiyao Coltd
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 Guangzhou Qingxintang Zhiyao Coltd
- Is Guangzhou Qingxintang Zhiyao Coltd on an FDA import alert?
- No listing for Guangzhou Qingxintang Zhiyao Coltd 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 Guangzhou Qingxintang Zhiyao Coltd?
- Yes. FDA refused 3 shipment lines from Guangzhou Qingxintang Zhiyao Coltd between November 10, 2020 and December 28, 2020. The most recent, on December 28, 2020, was dates, dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Guangzhou Qingxintang Zhiyao Coltd's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 3 lines).
- What is Guangzhou Qingxintang Zhiyao Coltd's FEI number?
- Guangzhou Qingxintang Zhiyao Coltd's FDA Establishment Identifier (FEI) is 3014127563.
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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.