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Nutribio

⚠️ Moderate Risk

FEI: 3009300584 • Doullens, Somme • FRANCE

FEI

FEI Number

3009300584

📍

Location

Doullens, Somme

🇫🇷

Country

FRANCE
🏢

Address

Zone Industrielle De Rouval, , Doullens, Somme, France

Moderate Risk

FDA Import Risk Assessment

36.5
LowModerateHighCritical

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

Statistics

4
Total Refusals
6
Unique Violations
10/23/2023
Latest Refusal
10/23/2023
Earliest Refusal

Score Breakdown

Violation Severity
41.3×40%
Refusal Volume
25.9×30%
Recency
41.0×20%
Frequency
40.0×10%
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

2603×

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.

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.

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.

3211×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

3281×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

Refusal History

DateProductViolationsDivision
10/23/2023
40PDY01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
260FALSE
Division of Southwest Imports (DSWI)
10/23/2023
40PDY01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
260FALSE
Division of Southwest Imports (DSWI)
10/23/2023
40PDY01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
260FALSE
Division of Southwest Imports (DSWI)
10/23/2023
40PDY01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is Nutribio's FDA import refusal history?

Nutribio (FEI: 3009300584) has 4 FDA import refusal record(s) in our database, spanning from 10/23/2023 to 10/23/2023.

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. Nutribio's FEI number is 3009300584.

What types of violations has Nutribio received?

Nutribio has been cited for 6 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 Nutribio come from?

All FDA import refusal data for Nutribio 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.