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DHD Pharma Inc.

Low Risk

FEI: 3014300557 • Delson, Quebec • CANADA

FEI

FEI Number

3014300557

📍

Location

Delson, Quebec

🇨🇦

Country

CANADA
🏢

Address

210-300 Ch Saint-Francois-Xavier, , Delson, Quebec, Canada

Low Risk

FDA Import Risk Assessment

18.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
2
Unique Violations
4/5/2019
Latest Refusal
4/5/2019
Earliest Refusal

Score Breakdown

Violation Severity
35.0×40%
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

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
4/5/2019
54YCA99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
274COLOR LBLG
320LACKS FIRM
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is DHD Pharma Inc.'s FDA import refusal history?

DHD Pharma Inc. (FEI: 3014300557) has 1 FDA import refusal record(s) in our database, spanning from 4/5/2019 to 4/5/2019.

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. DHD Pharma Inc.'s FEI number is 3014300557.

What types of violations has DHD Pharma Inc. received?

DHD Pharma Inc. has been cited for 2 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 DHD Pharma Inc. come from?

All FDA import refusal data for DHD Pharma 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.