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Shenzhen Chinalight Pam & Frank Industrial Co., Ltd.

⚠️ Moderate Risk

FEI: 3010581101 • Shenzhen Guangdong China • CHINA

FEI

FEI Number

3010581101

📍

Location

Shenzhen Guangdong China

🇨🇳

Country

CHINA
🏢

Address

Building A1, Pam & Frank Industrial, , Shenzhen Guangdong China, , China

Moderate Risk

FDA Import Risk Assessment

39.1
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
6/24/2014
Latest Refusal
6/24/2014
Earliest Refusal

Score Breakdown

Violation Severity
63.6×40%
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

23005×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

21204×

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.

24601×

UNSFDIETLB

The article appears to be a dietary supplement or contain a dietary ingredient that presents a significant or unreasonable risk of illness or injury under the conditions of use set out in the labeling or, if none are set out in the labeling, under customary conditions of use.

2511×

POISONOUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:

Refusal History

DateProductViolationsDivision
6/24/2014
54FCZ99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2300DIETARYLBL
2460UNSFDIETLB
251POISONOUS
Los Angeles District Office (LOS-DO)
6/24/2014
54FCZ99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2120UNSFDIETSP
2300DIETARYLBL
Los Angeles District Office (LOS-DO)
6/24/2014
54FCZ99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2120UNSFDIETSP
2300DIETARYLBL
Los Angeles District Office (LOS-DO)
6/24/2014
54FCZ99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2120UNSFDIETSP
2300DIETARYLBL
Los Angeles District Office (LOS-DO)
6/24/2014
54FBZ99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2120UNSFDIETSP
2300DIETARYLBL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Shenzhen Chinalight Pam & Frank Industrial Co., Ltd.'s FDA import refusal history?

Shenzhen Chinalight Pam & Frank Industrial Co., Ltd. (FEI: 3010581101) has 5 FDA import refusal record(s) in our database, spanning from 6/24/2014 to 6/24/2014.

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. Shenzhen Chinalight Pam & Frank Industrial Co., Ltd.'s FEI number is 3010581101.

What types of violations has Shenzhen Chinalight Pam & Frank Industrial Co., Ltd. received?

Shenzhen Chinalight Pam & Frank Industrial Co., Ltd. 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 Shenzhen Chinalight Pam & Frank Industrial Co., Ltd. come from?

All FDA import refusal data for Shenzhen Chinalight Pam & Frank Industrial Co., Ltd. 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.