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"Cem Technologys

⚠️ Moderate Risk

FEI: 3005646459 • Velikiy Novgorod, Novgorodskaya obl • RUSSIA

FEI

FEI Number

3005646459

📍

Location

Velikiy Novgorod, Novgorodskaya obl

🇷🇺

Country

RUSSIA
🏢

Address

Gagarin Avn. No.23 Bld 8, Office 208, , Velikiy Novgorod, Novgorodskaya obl, Russia

Moderate Risk

FDA Import Risk Assessment

27.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
7/6/2006
Latest Refusal
7/6/2006
Earliest Refusal

Score Breakdown

Violation Severity
57.5×40%
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

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).

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

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.

Refusal History

DateProductViolationsDivision
7/6/2006
80LDQDEVICE, GENERAL MEDICAL
118NOT LISTED
237NO PMA
341REGISTERED
508NO 510(K)
New York District Office (NYK-DO)

Frequently Asked Questions

What is "Cem Technologys's FDA import refusal history?

"Cem Technologys (FEI: 3005646459) has 1 FDA import refusal record(s) in our database, spanning from 7/6/2006 to 7/6/2006.

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. "Cem Technologys's FEI number is 3005646459.

What types of violations has "Cem Technologys received?

"Cem Technologys 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 "Cem Technologys come from?

All FDA import refusal data for "Cem Technologys 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.