Jiangyin Tianjiang Pharmaceutical Co.Ltd
⚠️ Moderate Risk
FEI: 3004268522 • Jiangyin, Jiangsu • CHINA
FEI Number
3004268522
Location
Jiangyin, Jiangsu
Country
CHINAAddress
1 Xinsheng Road, Jiangyin Economic Zone, Jiangyin, Jiangsu, 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
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
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:
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
NO ENGLISH
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
NCONTACTS
The product is a dietary supplement that is marketed in the United States and appears to not have a domestic address or domestic phone number through which the responsible person may receive a report of a serious adverse event.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
UNSFDIETSP
The article appears to be a dietary supplement or ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
DIETARYLBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.
EPHEDALK
The product is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a dietary supplement or a dietary ingredient that appears to contain ephedrine alkaloids, which presents an unreasonable risk of illness or injury under the conditions of use recommended or suggested in the labeling, or if no conditions of use are suggested in the labeling, under ordinary conditions of use.
LACKS FIRM
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/19/2013 | 54FBR20MINT (HERBAL & BOTANICALS, NOT TEAS - IF TEA FORM SEE 31P) | 3721PESTICIDE2 | Division of Northeast Imports (DNEI) |
| 7/19/2013 | 54FCR25SCHIZANDRA (HERBAL & BOTANICALS, NOT TEAS) | 3721PESTICIDE2 | Division of Northeast Imports (DNEI) |
| 5/21/2013 | 54F99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | Seattle District Office (SEA-DO) | |
| 1/4/2007 | 54ECR31ARISTOLOCHIA (FANGCHI), (HERBAL & BOTANICAL TEAS) | 251POISONOUS | Florida District Office (FLA-DO) |
| 1/4/2007 | 54ECR31ARISTOLOCHIA (FANGCHI), (HERBAL & BOTANICAL TEAS) | 251POISONOUS | Florida District Office (FLA-DO) |
| 1/4/2007 | 54ECR31ARISTOLOCHIA (FANGCHI), (HERBAL & BOTANICAL TEAS) | 251POISONOUS | Florida District Office (FLA-DO) |
| 3/3/2005 | 60CAR21EPHEDRINE (ADRENERGIC) | 75UNAPPROVED | Seattle District Office (SEA-DO) |
| 11/7/2003 | 54FBT99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | Los Angeles District Office (LOS-DO) | |
| 10/31/2003 | 46YG99FOOD ADDITIVES FOR HUMAN USE, N.E.C. | 238UNSAFE ADD | New York District Office (NYK-DO) |
| 10/31/2003 | 46YG99FOOD ADDITIVES FOR HUMAN USE, N.E.C. | 238UNSAFE ADD | New York District Office (NYK-DO) |
| 10/31/2003 | 46YG99FOOD ADDITIVES FOR HUMAN USE, N.E.C. | 238UNSAFE ADD | New York District Office (NYK-DO) |
| 10/31/2003 | 46YG99FOOD ADDITIVES FOR HUMAN USE, N.E.C. | 238UNSAFE ADD | New York District Office (NYK-DO) |
| 10/31/2003 | 46YG99FOOD ADDITIVES FOR HUMAN USE, N.E.C. | 238UNSAFE ADD | New York District Office (NYK-DO) |
| 4/18/2003 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Jiangyin Tianjiang Pharmaceutical Co.Ltd's FDA import refusal history?
Jiangyin Tianjiang Pharmaceutical Co.Ltd (FEI: 3004268522) has 14 FDA import refusal record(s) in our database, spanning from 4/18/2003 to 7/19/2013.
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. Jiangyin Tianjiang Pharmaceutical Co.Ltd's FEI number is 3004268522.
What types of violations has Jiangyin Tianjiang Pharmaceutical Co.Ltd received?
Jiangyin Tianjiang Pharmaceutical Co.Ltd has been cited for 14 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 Jiangyin Tianjiang Pharmaceutical Co.Ltd come from?
All FDA import refusal data for Jiangyin Tianjiang Pharmaceutical 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.