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Datrend Systems Inc.

⚠️ Moderate Risk

FEI: 3002806858 • Richmond, British Columbia • CANADA

FEI

FEI Number

3002806858

📍

Location

Richmond, British Columbia

🇨🇦

Country

CANADA
🏢

Address

5355 Parkwood Pl, , Richmond, British Columbia, Canada

Moderate Risk

FDA Import Risk Assessment

27.8
LowModerateHighCritical

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

Statistics

2
Total Refusals
5
Unique Violations
3/21/2013
Latest Refusal
2/29/2012
Earliest Refusal

Score Breakdown

Violation Severity
51.4×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
18.9×10%
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

1182×

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).

5082×

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.

2781×

NO TAG

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product to which is not affixed a certification in the form of a label or tag in conformity with section 534(h).

37411×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
3/21/2013
79ORKLASER ASSISTED LIPOLYSIS
118NOT LISTED
278NO TAG
3741FRNMFGREG
476NO REGISTR
508NO 510(K)
Seattle District Office (SEA-DO)
2/29/2012
74DPSELECTROCARDIOGRAPH
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Datrend Systems Inc.'s FDA import refusal history?

Datrend Systems Inc. (FEI: 3002806858) has 2 FDA import refusal record(s) in our database, spanning from 2/29/2012 to 3/21/2013.

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. Datrend Systems Inc.'s FEI number is 3002806858.

What types of violations has Datrend Systems Inc. received?

Datrend Systems Inc. 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 Datrend Systems Inc. come from?

All FDA import refusal data for Datrend Systems Inc. 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.