Hunan Tea Group Co., Ltd
FDA import alert and refusal historyChangsha, ChinaFEI 3009826660
Recorded by FDA as HUNAN TEA GROUP CO., LTD
As of October 26, 2026, Hunan Tea Group Co., Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 14, 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
- Tea, n.e.c. · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Hunan Tea Group Co., Ltd
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY1 refused line
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 Hunan Tea Group Co., Ltd
- Is Hunan Tea Group Co., Ltd on an FDA import alert?
- No listing for Hunan Tea Group 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 China page.
- Has FDA refused shipments from Hunan Tea Group Co., Ltd?
- Yes. FDA refused 1 shipment line from Hunan Tea Group Co., Ltd on March 14, 2018. The most recent, on March 14, 2018, was tea, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Hunan Tea Group Co., Ltd's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- When was Hunan Tea Group Co., Ltd last inspected by FDA?
- FDA's most recent inspection of Hunan Tea Group Co., Ltd with a final classification is dated August 4, 2026 and was classified NAI (No Action Indicated).
- What is Hunan Tea Group Co., Ltd's FEI number?
- Hunan Tea Group Co., Ltd's FDA Establishment Identifier (FEI) is 3009826660.
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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.