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SUNYATA PRODUTOS ALTERNATIVOS LTDA

✅ Low Risk

FEI: 3003998351 • Atibaia, Sao Paulo • BRAZIL

FEI

FEI Number

3003998351

📍

Location

Atibaia, Sao Paulo

🇧🇷

Country

BRAZIL
🏢

Address

Avenida Presidente Vargas, 334, , Atibaia, Sao Paulo, Brazil

Low Risk

FDA Import Risk Assessment

22.6
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

3
Total Refusals
5
Unique Violations
6/18/2012
Latest Refusal
7/11/2007
Earliest Refusal

Score Breakdown

Violation Severity
38.3×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
6.1×10%
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.

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.

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.

4731×

LABELING

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

Refusal History

DateProductViolationsDivision
6/18/2012
54FAK99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
320LACKS FIRM
473LABELING
482NUTRIT LBL
New Orleans District Office (NOL-DO)
1/3/2011
54FAY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
260FALSE
New Orleans District Office (NOL-DO)
7/11/2007
28CYT99NATURAL EXTRACT OR FLAVOR, N.E.C.
321LACKS N/C
482NUTRIT LBL
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is SUNYATA PRODUTOS ALTERNATIVOS LTDA's FDA import refusal history?

SUNYATA PRODUTOS ALTERNATIVOS LTDA (FEI: 3003998351) has 3 FDA import refusal record(s) in our database, spanning from 7/11/2007 to 6/18/2012.

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. SUNYATA PRODUTOS ALTERNATIVOS LTDA's FEI number is 3003998351.

What types of violations has SUNYATA PRODUTOS ALTERNATIVOS LTDA received?

SUNYATA PRODUTOS ALTERNATIVOS LTDA 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 SUNYATA PRODUTOS ALTERNATIVOS LTDA come from?

All FDA import refusal data for SUNYATA PRODUTOS ALTERNATIVOS LTDA 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.