ImportRefusal LogoImportRefusal

Qingdao Qinzeyuan Biotechnology Co., Ltd.

⚠️ Moderate Risk

FEI: 3030901985 • Qingdao, Shandong • CHINA

FEI

FEI Number

3030901985

📍

Location

Qingdao, Shandong

🇨🇳

Country

CHINA
🏢

Address

No. 33 Zhengyuan Road, High Tech Zone, Qingdao, Shandong, China

Moderate Risk

FDA Import Risk Assessment

40.9
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
12/23/2024
Latest Refusal
12/23/2024
Earliest Refusal

Score Breakdown

Violation Severity
52.0×40%
Refusal Volume
11.2×30%
Recency
78.7×20%
Frequency
10.0×10%
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

1181×

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).

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.

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.

4831×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

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).

Refusal History

DateProductViolationsDivision
12/23/2024
56FDZ99PEPTIDE N.E.C.
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Qingdao Qinzeyuan Biotechnology Co., Ltd.'s FDA import refusal history?

Qingdao Qinzeyuan Biotechnology Co., Ltd. (FEI: 3030901985) has 1 FDA import refusal record(s) in our database, spanning from 12/23/2024 to 12/23/2024.

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. Qingdao Qinzeyuan Biotechnology Co., Ltd.'s FEI number is 3030901985.

What types of violations has Qingdao Qinzeyuan Biotechnology Co., Ltd. received?

Qingdao Qinzeyuan Biotechnology 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 Qingdao Qinzeyuan Biotechnology Co., Ltd. come from?

All FDA import refusal data for Qingdao Qinzeyuan Biotechnology 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.