ImportRefusal LogoImportRefusal

Rodzon Marketing Corporation

⚠️ Moderate Risk

FEI: 2000009240 • Pasay City, National Capital Region • PHILIPPINES

FEI

FEI Number

2000009240

📍

Location

Pasay City, National Capital Region

🇵🇭
🏢

Address

2451 Lakandula, St., Pasay City, National Capital Region, Philippines

Moderate Risk

FDA Import Risk Assessment

40.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
3/24/2025
Latest Refusal
7/3/2012
Earliest Refusal

Score Breakdown

Violation Severity
48.3×40%
Refusal Volume
22.3×30%
Recency
68.9×20%
Frequency
2.4×10%
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

38862×

FSVP VIO

The article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) in that it appears that the importer (as defined in section 805 of the FD&C Act) is in violation of section 805.

2181×

LIST INGRE

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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

2561×

INCONSPICU

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

33201×

TRANSFAT

The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].

Refusal History

DateProductViolationsDivision
3/24/2025
25LFH24GINGER ROOT, DRIED OR PASTE
3886FSVP VIO
Division of Southwest Imports (DSWI)
3/24/2025
25LFH24GINGER ROOT, DRIED OR PASTE
3886FSVP VIO
Division of Southwest Imports (DSWI)
7/3/2012
23ECT05COCONUT, SPREAD
218LIST INGRE
256INCONSPICU
260FALSE
3320TRANSFAT
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Rodzon Marketing Corporation's FDA import refusal history?

Rodzon Marketing Corporation (FEI: 2000009240) has 3 FDA import refusal record(s) in our database, spanning from 7/3/2012 to 3/24/2025.

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. Rodzon Marketing Corporation's FEI number is 2000009240.

What types of violations has Rodzon Marketing Corporation received?

Rodzon Marketing Corporation 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 Rodzon Marketing Corporation come from?

All FDA import refusal data for Rodzon Marketing Corporation 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.