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Mediamerica Sa

✅ Low Risk

FEI: 3007116917 • Los Prados • DOMINICAN REPUBLIC

FEI

FEI Number

3007116917

📍

Location

Los Prados

🇩🇴
🏢

Address

Ave Nunez De Cacceres No 62, , Los Prados, , Dominican Republic

Low Risk

FDA Import Risk Assessment

20.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
10/2/2008
Latest Refusal
10/2/2008
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
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

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

4741×

COSMETLBLG

It appears the label does not bear the common or usual name of the cosmetic.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

Refusal History

DateProductViolationsDivision
10/2/2008
53LD99OTHER SKIN CARE PREPARATIONS, N.E.C.
471CSTIC LBLG
474COSMETLBLG
475COSMETLBLG
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Mediamerica Sa's FDA import refusal history?

Mediamerica Sa (FEI: 3007116917) has 1 FDA import refusal record(s) in our database, spanning from 10/2/2008 to 10/2/2008.

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. Mediamerica Sa's FEI number is 3007116917.

What types of violations has Mediamerica Sa received?

Mediamerica Sa has been cited for 3 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 Mediamerica Sa come from?

All FDA import refusal data for Mediamerica Sa 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.