ImportRefusal LogoImportRefusal

Casa Chapa S.A. De C.V.

✅ Low Risk

FEI: 3004423100 • Monterrey, Nuevo Leon • MEXICO

FEI

FEI Number

3004423100

📍

Location

Monterrey, Nuevo Leon

🇲🇽

Country

MEXICO
🏢

Address

Avenida Fidel Velazquez No. 1513, Local 5-F; Col. CENTRAL, Monterrey, Nuevo Leon, Mexico

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
7/21/2002
Latest Refusal
7/21/2002
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

2541×

STD QUALIT

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(h)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a standard of quality has been prescribed by regulation as provided by Section 401 of the FD&C Act, and its quality falls below such standard and its label does not bear a statement that it falls below such standard in such manner and form as such regulations specify.

3241×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

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
7/21/2002
02EFT05WHEAT FLOUR, ENRICHED (ALL PURPOSE)
254STD QUALIT
324NO ENGLISH
482NUTRIT LBL
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Casa Chapa S.A. De C.V.'s FDA import refusal history?

Casa Chapa S.A. De C.V. (FEI: 3004423100) has 1 FDA import refusal record(s) in our database, spanning from 7/21/2002 to 7/21/2002.

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. Casa Chapa S.A. De C.V.'s FEI number is 3004423100.

What types of violations has Casa Chapa S.A. De C.V. received?

Casa Chapa S.A. De C.V. 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 Casa Chapa S.A. De C.V. come from?

All FDA import refusal data for Casa Chapa S.A. De C.V. 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.