ImportRefusal LogoImportRefusal

Yumen Qianhua Pharmaceutical Co., Ltd.

⚠️ Moderate Risk

FEI: 3030638441 • Jiuquan, Gansu • CHINA

FEI

FEI Number

3030638441

📍

Location

Jiuquan, Gansu

🇨🇳

Country

CHINA
🏢

Address

Old, No. 8 Sanba Road; Yumen, Jiuquan, Gansu, China

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

4
Total Refusals
3
Unique Violations
8/15/2018
Latest Refusal
6/22/2011
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
5.6×10%
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

1184×

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).

32802×

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.

752×

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).

Refusal History

DateProductViolationsDivision
8/15/2018
66KCT01METHIMAZOLE (THYROID INHIBITOR)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/24/2018
62CDL41MINOXIDIL (ANTI-HYPERTENSIVE)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Northern Border Imports (DNBI)
8/2/2013
60QCT70TETRACAINE (ANESTHETIC)
118NOT LISTED
Cincinnati District Office (CIN-DO)
6/22/2011
66KCS01METHIMAZOLE (THYROID INHIBITOR)
118NOT LISTED
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Yumen Qianhua Pharmaceutical Co., Ltd.'s FDA import refusal history?

Yumen Qianhua Pharmaceutical Co., Ltd. (FEI: 3030638441) has 4 FDA import refusal record(s) in our database, spanning from 6/22/2011 to 8/15/2018.

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. Yumen Qianhua Pharmaceutical Co., Ltd.'s FEI number is 3030638441.

What types of violations has Yumen Qianhua Pharmaceutical Co., Ltd. received?

Yumen Qianhua Pharmaceutical Co., Ltd. has been cited for 3 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 Yumen Qianhua Pharmaceutical Co., Ltd. come from?

All FDA import refusal data for Yumen Qianhua 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.