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Fresh

Low Risk

FEI: 3005700947 • Paris, Paris • FRANCE

FEI

FEI Number

3005700947

📍

Location

Paris, Paris

🇫🇷

Country

FRANCE
🏢

Address

18 B avenue Hoche, , Paris, Paris, France

Low Risk

FDA Import Risk Assessment

23.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
1/3/2019
Latest Refusal
1/3/2019
Earliest Refusal

Score Breakdown

Violation Severity
48.0×40%
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

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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

4721×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

Refusal History

DateProductViolationsDivision
1/3/2019
66PAO14OCTINOXATE (ULTRAVIOLET SCREEN/SUNSCREEN)
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
336INCONSPICU
472NO ENGLISH
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Fresh's FDA import refusal history?

Fresh (FEI: 3005700947) has 1 FDA import refusal record(s) in our database, spanning from 1/3/2019 to 1/3/2019.

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. Fresh's FEI number is 3005700947.

What types of violations has Fresh received?

Fresh 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 Fresh come from?

All FDA import refusal data for Fresh 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.