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QINGDAO XINRUN EYELASH GLUE CO.LTD

⚠️ Moderate Risk

FEI: 3020777589 • Pingdu City • CHINA

FEI

FEI Number

3020777589

📍

Location

Pingdu City

🇨🇳

Country

CHINA
🏢

Address

No 109, Changle Industrial Park, , Pingdu City, , China

Moderate Risk

FDA Import Risk Assessment

37.1
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
6/8/2022
Latest Refusal
5/19/2022
Earliest Refusal

Score Breakdown

Violation Severity
62.0×40%
Refusal Volume
22.3×30%
Recency
13.2×20%
Frequency
30.0×10%
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

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).

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).

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

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.

Refusal History

DateProductViolationsDivision
6/8/2022
87MOZACID, HYALURONIC, INTRAARTICULAR
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/6/2022
60QAJ07LIDOCAINE
118NOT LISTED
3260NO ENGLISH
3280FRNMFGREG
Division of Southeast Imports (DSEI)
5/19/2022
65QCZ02BOTOX
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is QINGDAO XINRUN EYELASH GLUE CO.LTD's FDA import refusal history?

QINGDAO XINRUN EYELASH GLUE CO.LTD (FEI: 3020777589) has 3 FDA import refusal record(s) in our database, spanning from 5/19/2022 to 6/8/2022.

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 XINRUN EYELASH GLUE CO.LTD's FEI number is 3020777589.

What types of violations has QINGDAO XINRUN EYELASH GLUE CO.LTD received?

QINGDAO XINRUN EYELASH GLUE CO.LTD has been cited for 4 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 XINRUN EYELASH GLUE CO.LTD come from?

All FDA import refusal data for QINGDAO XINRUN EYELASH GLUE 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.