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Minsheng Group Shaoxing Pharmaceutical Co., Ltd.

⚠️ Moderate Risk

FEI: 3004986788 • Shaoxing, Zhejiang • CHINA

FEI

FEI Number

3004986788

📍

Location

Shaoxing, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

No. 315 Tanggong Road, Paojiang Industrial Zone, , Shaoxing, Zhejiang, China

Moderate Risk

FDA Import Risk Assessment

38.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

5
Total Refusals
5
Unique Violations
1/19/2023
Latest Refusal
3/30/2011
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
28.8×30%
Recency
25.9×20%
Frequency
4.2×10%
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

1182×

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).

161×

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.

22801×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

32801×

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.

721×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

Refusal History

DateProductViolationsDivision
1/19/2023
60ZOR32PYRANTEL PAMOATE (ANTIPARASITIC)
2280DIRSEXMPT
Division of Northeast Imports (DNEI)
10/19/2020
60ZCT32PYRANTEL PAMOATE (ANTIPARASITIC)
3280FRNMFGREG
Division of Southeast Imports (DSEI)
2/13/2013
56YJS99ANTIBIOTIC N.E.C.
72NEW VET DR
New Orleans District Office (NOL-DO)
8/8/2011
56YJS99ANTIBIOTIC N.E.C.
118NOT LISTED
16DIRECTIONS
Southwest Import District Office (SWI-DO)
3/30/2011
60WAS31PYRANTEL PAMOATE (ANTHELMINTIC)
118NOT LISTED
New York District Office (NYK-DO)

Frequently Asked Questions

What is Minsheng Group Shaoxing Pharmaceutical Co., Ltd.'s FDA import refusal history?

Minsheng Group Shaoxing Pharmaceutical Co., Ltd. (FEI: 3004986788) has 5 FDA import refusal record(s) in our database, spanning from 3/30/2011 to 1/19/2023.

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. Minsheng Group Shaoxing Pharmaceutical Co., Ltd.'s FEI number is 3004986788.

What types of violations has Minsheng Group Shaoxing Pharmaceutical Co., Ltd. received?

Minsheng Group Shaoxing Pharmaceutical Co., Ltd. has been cited for 5 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 Minsheng Group Shaoxing Pharmaceutical Co., Ltd. come from?

All FDA import refusal data for Minsheng Group Shaoxing 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.