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DANYANG JIECHENG ELECTRONICS CO.

⚠️ Moderate Risk

FEI: 3012603749 • Danyang • CHINA

FEI

FEI Number

3012603749

📍

Location

Danyang

🇨🇳

Country

CHINA
🏢

Address

N 3p No.6 Liyao East Rd, , Danyang, , China

Moderate Risk

FDA Import Risk Assessment

29.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
6
Unique Violations
8/25/2016
Latest Refusal
8/25/2016
Earliest Refusal

Score Breakdown

Violation Severity
63.3×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

1171×

DANGEROUS

The article appears to be dangerous to health when used in the dosage or manner, or with the frequency or duration, prescribed, recommended, or suggested in the labeling thereof.

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.

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.

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
8/25/2016
79MVFSYSTEM, LASER, PHOTODYNAMIC THERAPY
117DANGEROUS
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
84RX DEVICE
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is DANYANG JIECHENG ELECTRONICS CO.'s FDA import refusal history?

DANYANG JIECHENG ELECTRONICS CO. (FEI: 3012603749) has 1 FDA import refusal record(s) in our database, spanning from 8/25/2016 to 8/25/2016.

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. DANYANG JIECHENG ELECTRONICS CO.'s FEI number is 3012603749.

What types of violations has DANYANG JIECHENG ELECTRONICS CO. received?

DANYANG JIECHENG ELECTRONICS CO. has been cited for 6 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 DANYANG JIECHENG ELECTRONICS CO. come from?

All FDA import refusal data for DANYANG JIECHENG ELECTRONICS CO. 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.