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Changzhou Sunlight Pharmaceutical Co., Ltd.

⚠️ Moderate Risk

FEI: 3003662818 • Changzhou, Jiangsu • CHINA

FEI

FEI Number

3003662818

📍

Location

Changzhou, Jiangsu

🇨🇳

Country

CHINA
🏢

Address

Benniu, No. 216 Yunnan West Rd; Town, Xinbei, Changzhou, Jiangsu, China

Moderate Risk

FDA Import Risk Assessment

33.3
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
6/4/2013
Latest Refusal
7/8/2010
Earliest Refusal

Score Breakdown

Violation Severity
64.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
10.3×10%
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

162×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

721×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

Refusal History

DateProductViolationsDivision
6/4/2013
60QAY56BENZOCAINE (ANESTHETIC)
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
New York District Office (NYK-DO)
9/21/2011
60QJS56BENZOCAINE (ANESTHETIC)
72NEW VET DR
New York District Office (NYK-DO)
7/8/2010
60QAR56BENZOCAINE (ANESTHETIC)
16DIRECTIONS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Changzhou Sunlight Pharmaceutical Co., Ltd.'s FDA import refusal history?

Changzhou Sunlight Pharmaceutical Co., Ltd. (FEI: 3003662818) has 3 FDA import refusal record(s) in our database, spanning from 7/8/2010 to 6/4/2013.

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. Changzhou Sunlight Pharmaceutical Co., Ltd.'s FEI number is 3003662818.

What types of violations has Changzhou Sunlight Pharmaceutical Co., Ltd. received?

Changzhou Sunlight Pharmaceutical 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 Changzhou Sunlight Pharmaceutical Co., Ltd. come from?

All FDA import refusal data for Changzhou Sunlight Pharmaceutical 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.