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Salvema

⚠️ Moderate Risk

FEI: 3009164656 • Agadir, Agadir Ida Ou Tanan • MOROCCO

FEI

FEI Number

3009164656

📍

Location

Agadir, Agadir Ida Ou Tanan

🇲🇦

Country

MOROCCO
🏢

Address

Zone Industrielle D'Ait Melloul80-152 Bp, , Agadir, Agadir Ida Ou Tanan, Morocco

Moderate Risk

FDA Import Risk Assessment

32.0
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
4/1/2013
Latest Refusal
4/1/2013
Earliest Refusal

Score Breakdown

Violation Severity
50.7×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
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

4734×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

4824×

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.

834×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

3282×

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.

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.

Refusal History

DateProductViolationsDivision
4/1/2013
39YHT99PREPARED SALAD, N.E.C.
473LABELING
482NUTRIT LBL
83NO PROCESS
New York District Office (NYK-DO)
4/1/2013
39YHT99PREPARED SALAD, N.E.C.
473LABELING
482NUTRIT LBL
83NO PROCESS
New York District Office (NYK-DO)
4/1/2013
39YHT99PREPARED SALAD, N.E.C.
328USUAL NAME
473LABELING
482NUTRIT LBL
83NO PROCESS
New York District Office (NYK-DO)
4/1/2013
39YHT99PREPARED SALAD, N.E.C.
218LIST INGRE
328USUAL NAME
473LABELING
482NUTRIT LBL
83NO PROCESS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Salvema's FDA import refusal history?

Salvema (FEI: 3009164656) has 4 FDA import refusal record(s) in our database, spanning from 4/1/2013 to 4/1/2013.

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. Salvema's FEI number is 3009164656.

What types of violations has Salvema received?

Salvema 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 Salvema come from?

All FDA import refusal data for Salvema 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.