ImportRefusal LogoImportRefusal

Chaivinit Enterprise

⚠️ Moderate Risk

FEI: 3009402372 • Penang, Pulau Pinang • MALAYSIA

FEI

FEI Number

3009402372

📍

Location

Penang, Pulau Pinang

🇲🇾

Country

MALAYSIA
🏢

Address

7 Taman Air Rajah, , Penang, Pulau Pinang, Malaysia

Moderate Risk

FDA Import Risk Assessment

31.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
1/16/2014
Latest Refusal
11/7/2013
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

21202×

UNSFDIETSP

The article appears to be a dietary supplement or ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury.

32602×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

2561×

INCONSPICU

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)).

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.

Refusal History

DateProductViolationsDivision
1/16/2014
54FYR99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
260FALSE
Cincinnati District Office (CIN-DO)
1/16/2014
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
256INCONSPICU
Cincinnati District Office (CIN-DO)
11/7/2013
50NHH18HENNA
2120UNSFDIETSP
3260NO ENGLISH
Los Angeles District Office (LOS-DO)
11/7/2013
50NHH18HENNA
2120UNSFDIETSP
3260NO ENGLISH
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Chaivinit Enterprise's FDA import refusal history?

Chaivinit Enterprise (FEI: 3009402372) has 4 FDA import refusal record(s) in our database, spanning from 11/7/2013 to 1/16/2014.

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. Chaivinit Enterprise's FEI number is 3009402372.

What types of violations has Chaivinit Enterprise received?

Chaivinit Enterprise 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 Chaivinit Enterprise come from?

All FDA import refusal data for Chaivinit Enterprise 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.