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Changsha Huir Biological-Tech Co., Ltd

⚠️ High Risk

FEI: 3013409304 • Changsha, Hunan • CHINA

FEI

FEI Number

3013409304

📍

Location

Changsha, Hunan

🇨🇳

Country

CHINA
🏢

Address

Jindan Mansion, 1 Xiongtian Rd, Changsha, Hunan, China

High Risk

FDA Import Risk Assessment

50.7
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

15
Total Refusals
12
Unique Violations
5/30/2023
Latest Refusal
9/1/2009
Earliest Refusal

Score Breakdown

Violation Severity
67.1×40%
Refusal Volume
44.6×30%
Recency
47.2×20%
Frequency
10.9×10%
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

1185×

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).

32804×

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.

164×

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.

2382×

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.

37212×

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:

3331×

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.

34221×

UNFIT4FOOD

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be unfit for food.

751×

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).

2411×

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:

2511×

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:

29201×

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:

31401×

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

DateProductViolationsDivision
5/30/2023
54FBT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
251POISONOUS
3422UNFIT4FOOD
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)
118NOT LISTED
3280FRNMFGREG
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)
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
Cincinnati District Office (CIN-DO)
4/6/2016
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
Cincinnati District Office (CIN-DO)
9/16/2015
60RIY18ORLISTAT/TETRAHYDROLIPSTATIN (ANOREXIC)
118NOT LISTED
3280FRNMFGREG
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.
16DIRECTIONS
333LACKS FIRM
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)
118NOT LISTED
16DIRECTIONS
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.