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GRUPO BOTANICO NAYEC SA DE CV

⚠️ Moderate Risk

FEI: 3013135411 • Ciudad De Mexico, Ciudad de Mexico • MEXICO

FEI

FEI Number

3013135411

📍

Location

Ciudad De Mexico, Ciudad de Mexico

🇲🇽

Country

MEXICO
🏢

Address

Espana 423, Col. San Juan Xalpa, Iztapalapa, Ciudad De Mexico, Ciudad de Mexico, Mexico

Moderate Risk

FDA Import Risk Assessment

34.5
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
2/5/2016
Latest Refusal
5/20/2015
Earliest Refusal

Score Breakdown

Violation Severity
52.0×40%
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

4822×

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.

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.

2601×

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.

751×

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).

Refusal History

DateProductViolationsDivision
2/5/2016
54FDT32ARNICA (HERBAL & BOTANICALS, NOT TEAS)
218LIST INGRE
Southwest Import District Office (SWI-DO)
1/8/2016
54FBH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Southwest Import District Office (SWI-DO)
11/13/2015
41BGF99FOODS WITH SUPPLEMENTAL NUTRIENTS ADDED, WITH OR WITHOUT ARTIFICAL SWEETNERS
260FALSE
Southwest Import District Office (SWI-DO)
5/20/2015
41BGF99FOODS WITH SUPPLEMENTAL NUTRIENTS ADDED, WITH OR WITHOUT ARTIFICAL SWEETNERS
482NUTRIT LBL
Southwest Import District Office (SWI-DO)
5/20/2015
41BGF99FOODS WITH SUPPLEMENTAL NUTRIENTS ADDED, WITH OR WITHOUT ARTIFICAL SWEETNERS
482NUTRIT LBL
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is GRUPO BOTANICO NAYEC SA DE CV's FDA import refusal history?

GRUPO BOTANICO NAYEC SA DE CV (FEI: 3013135411) has 5 FDA import refusal record(s) in our database, spanning from 5/20/2015 to 2/5/2016.

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. GRUPO BOTANICO NAYEC SA DE CV's FEI number is 3013135411.

What types of violations has GRUPO BOTANICO NAYEC SA DE CV received?

GRUPO BOTANICO NAYEC SA DE CV has been cited for 4 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 GRUPO BOTANICO NAYEC SA DE CV come from?

All FDA import refusal data for GRUPO BOTANICO NAYEC SA DE CV 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.