Zhejiang Tea Import & Export Co., Ltd.
⚠️ Moderate Risk
FEI: 3004920454 • Hangzhou, Zhejiang • CHINA
FEI Number
3004920454
Location
Hangzhou, Zhejiang
Country
CHINAAddress
218 Tiyuchang Road, , Hangzhou, Zhejiang, China
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
PESTICIDE2
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
HEALTH C
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling bears an unauthorized nutrient content/health claim.
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/26/2015 | 25RGH01MUSHROOM, COMMON (AGARICUS BISPORUS), BROKEN OR KIBBLED | 249FILTHY | San Francisco District Office (SAN-DO) |
| 9/9/2013 | 31PFH04TEA, CAMOMILLE, CHAMOMILE (TEA SUBSTITUTE) | 3721PESTICIDE2 | Florida District Office (FLA-DO) |
| 9/6/2013 | 31PGT99TEA SUBSTITUTES, N.E.C. | 3721PESTICIDE2 | Los Angeles District Office (LOS-DO) |
| 6/18/2008 | 31KGH02TEA, GREEN | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
| 4/28/2008 | 31KFE03TEA, OOLONG | Los Angeles District Office (LOS-DO) | |
| 8/2/2007 | 66VAY99MISCELLANEOUS PATENT MEDICINES, ETC. | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 2/10/2006 | 25SGH01MUSHROOM, COMMON (AGARICUS BISPORUS), FUNGI PRODUCTS, N.E.C. | 249FILTHY | Division of West Coast Imports (DWCI) |
| 1/9/2006 | 25PGH01MUSHROOM, COMMON (AGARICUS BISPORUS), WHOLE (BUTTON) (FUNGI) | 249FILTHY | Division of West Coast Imports (DWCI) |
| 1/9/2006 | 25PGH01MUSHROOM, COMMON (AGARICUS BISPORUS), WHOLE (BUTTON) (FUNGI) | 249FILTHY | Division of West Coast Imports (DWCI) |
| 3/11/2004 | 25MGP07RADISH, JUICE OR DRINK | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Zhejiang Tea Import & Export Co., Ltd.'s FDA import refusal history?
Zhejiang Tea Import & Export Co., Ltd. (FEI: 3004920454) has 10 FDA import refusal record(s) in our database, spanning from 3/11/2004 to 3/26/2015.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Zhejiang Tea Import & Export Co., Ltd.'s FEI number is 3004920454.
What types of violations has Zhejiang Tea Import & Export Co., Ltd. received?
Zhejiang Tea Import & Export Co., Ltd. has been cited for 8 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Zhejiang Tea Import & Export Co., Ltd. come from?
All FDA import refusal data for Zhejiang Tea Import & Export Co., Ltd. is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.