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Shandong Lukang Pharmaceutical Co. Ltd.

⚠️ Moderate Risk

FEI: 3002664271 • Zoucheng, Shandong • CHINA

FEI

FEI Number

3002664271

📍

Location

Zoucheng, Shandong

🇨🇳

Country

CHINA
🏢

Address

Zoucheng Industrial Park, 99 Hualu Road, Zoucheng, Shandong, China

Moderate Risk

FDA Import Risk Assessment

39.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
10/20/2016
Latest Refusal
11/14/2006
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
3.0×10%
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

161×

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.

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.

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
10/20/2016
56LCS72TYLOSIN TARTRATE (NON-CERTIFIABLE)
75UNAPPROVED
Division of Northeast Imports (DNEI)
4/15/2013
56BCR54NATAMYCIN (PENICILLIN, SYNTHETICALLY PRODUCED)
16DIRECTIONS
Seattle District Office (SEA-DO)
11/14/2006
56LXK72TYLOSIN TARTRATE (NON-CERTIFIABLE)
72NEW VET DR
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Shandong Lukang Pharmaceutical Co. Ltd.'s FDA import refusal history?

Shandong Lukang Pharmaceutical Co. Ltd. (FEI: 3002664271) has 3 FDA import refusal record(s) in our database, spanning from 11/14/2006 to 10/20/2016.

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. Shandong Lukang Pharmaceutical Co. Ltd.'s FEI number is 3002664271.

What types of violations has Shandong Lukang Pharmaceutical Co. Ltd. received?

Shandong Lukang Pharmaceutical Co. Ltd. has been cited for 3 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 Shandong Lukang Pharmaceutical Co. Ltd. come from?

All FDA import refusal data for Shandong Lukang 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.