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Servicios De Manufactura Int'L S De Rl

⚠️ Moderate Risk

FEI: 3005660649 • Cd Juarez • MEXICO

FEI

FEI Number

3005660649

📍

Location

Cd Juarez

🇲🇽

Country

MEXICO
🏢

Address

Paseo De La Victoria #9450, , Cd Juarez, , Mexico

Moderate Risk

FDA Import Risk Assessment

33.6
LowModerateHighCritical

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

Statistics

5
Total Refusals
5
Unique Violations
7/11/2007
Latest Refusal
7/11/2007
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

2185×

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.

3205×

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.

755×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

4733×

LABELING

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

3352×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

Refusal History

DateProductViolationsDivision
7/11/2007
54YCR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
320LACKS FIRM
473LABELING
75UNAPPROVED
Southwest Import District Office (SWI-DO)
7/11/2007
54YCR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
320LACKS FIRM
473LABELING
75UNAPPROVED
Southwest Import District Office (SWI-DO)
7/11/2007
54YCR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
320LACKS FIRM
473LABELING
75UNAPPROVED
Southwest Import District Office (SWI-DO)
7/11/2007
54YCR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
320LACKS FIRM
335LACKS N/C
75UNAPPROVED
Southwest Import District Office (SWI-DO)
7/11/2007
54YCR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
320LACKS FIRM
335LACKS N/C
75UNAPPROVED
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Servicios De Manufactura Int'L S De Rl's FDA import refusal history?

Servicios De Manufactura Int'L S De Rl (FEI: 3005660649) has 5 FDA import refusal record(s) in our database, spanning from 7/11/2007 to 7/11/2007.

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. Servicios De Manufactura Int'L S De Rl's FEI number is 3005660649.

What types of violations has Servicios De Manufactura Int'L S De Rl received?

Servicios De Manufactura Int'L S De Rl 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 Servicios De Manufactura Int'L S De Rl come from?

All FDA import refusal data for Servicios De Manufactura Int'L S De Rl 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.