Changsha Huir Biological-Tech Co., Ltd
⚠️ High Risk
FEI: 3013409304 • Changsha, Hunan • CHINA
FEI Number
3013409304
Location
Changsha, Hunan
Country
CHINAAddress
Jindan Mansion, 1 Xiongtian Rd, Changsha, Hunan, China
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
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).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
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.
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:
LACKS FIRM
The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.
UNFIT4FOOD
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be unfit for food.
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).
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
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:
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:
SBGINSENG
The article is subject to refusal of admission in that it appears to be Misbranded because it or its ingredients purport to be or are represented as Ginseng, but are not an herb or herbal ingredient derived from a plant classified within the genus Panax.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/30/2023 | 54FBT99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | Division of Northeast Imports (DNEI) | |
| 4/20/2018 | 54FBR12GINSENG (HERBAL & BOTANICALS, NOT TEAS) | 3140SBGINSENG | Division of West Coast Imports (DWCI) |
| 11/28/2017 | 64LAR58PREGNENOLONE SUCCINATE (GLUCOCORTICOID) | Division of Southeast Imports (DSEI) | |
| 6/26/2017 | 54FBR33ASTRAGALUS (MILK VETCH ROOT), (HERBAL & BOTANICALS, NOT TEAS) | 241PESTICIDE | Division of West Coast Imports (DWCI) |
| 4/8/2016 | 62JCS09LEVODOPA (ANTI-PARKINSONIAN) | Cincinnati District Office (CIN-DO) | |
| 4/6/2016 | 66VCY99MISCELLANEOUS PATENT MEDICINES, ETC. | Cincinnati District Office (CIN-DO) | |
| 9/16/2015 | 60RIY18ORLISTAT/TETRAHYDROLIPSTATIN (ANOREXIC) | Cincinnati District Office (CIN-DO) | |
| 3/17/2015 | 54FYT33ASTRAGALUS (MILK VETCH ROOT), (HERBAL & BOTANICALS, NOT TEAS) | 3721PESTICIDE2 | Southwest Import District Office (SWI-DO) |
| 3/17/2015 | 54FYT99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | 3721PESTICIDE2 | Southwest Import District Office (SWI-DO) |
| 2/21/2014 | 62JCR99ANTI-PARKINSONIAN N.E.C. | New Orleans District Office (NOL-DO) | |
| 2/7/2012 | 20FGB24WOLFBERRY (CHINESE OR SOUTHEAST ASIAN BERRY OF THE CHINESE MATRIMONY VINE, W/SLIGHT LICORICE FLAVOR) | 238UNSAFE ADD | Detroit District Office (DET-DO) |
| 2/7/2012 | 20FGB24WOLFBERRY (CHINESE OR SOUTHEAST ASIAN BERRY OF THE CHINESE MATRIMONY VINE, W/SLIGHT LICORICE FLAVOR) | 238UNSAFE ADD | Detroit District Office (DET-DO) |
| 7/21/2011 | 20BGT99BERRIES, DRIED OR PASTE, N.E.C. | 2920PESTICIDES | Los Angeles District Office (LOS-DO) |
| 7/6/2011 | 65A99MEMORY ADJUVANT, N.E.C. | 75UNAPPROVED | Seattle District Office (SEA-DO) |
| 9/1/2009 | 62JIS09LEVODOPA (ANTI-PARKINSONIAN) | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Changsha Huir Biological-Tech Co., Ltd's FDA import refusal history?
Changsha Huir Biological-Tech Co., Ltd (FEI: 3013409304) has 15 FDA import refusal record(s) in our database, spanning from 9/1/2009 to 5/30/2023.
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. Changsha Huir Biological-Tech Co., Ltd's FEI number is 3013409304.
What types of violations has Changsha Huir Biological-Tech Co., Ltd received?
Changsha Huir Biological-Tech Co., Ltd has been cited for 12 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 Changsha Huir Biological-Tech Co., Ltd come from?
All FDA import refusal data for Changsha Huir Biological-Tech 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.