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Whenzhou Pharmaceutical Factory (Offices)

⚠️ Moderate Risk

FEI: 3002603232 • Wenzhou • CHINA

FEI

FEI Number

3002603232

📍

Location

Wenzhou

🇨🇳

Country

CHINA
🏢

Address

Kangle Bldg. Rm. 504 F/5, No. 112 Ma An Chi Road (West), Wenzhou, , China

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
6/1/2006
Latest Refusal
6/1/2006
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

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).

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.

Refusal History

DateProductViolationsDivision
6/1/2006
60LBS01ACETAMINOPHEN (ANALGESIC)
118NOT LISTED
16DIRECTIONS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Whenzhou Pharmaceutical Factory (Offices)'s FDA import refusal history?

Whenzhou Pharmaceutical Factory (Offices) (FEI: 3002603232) has 1 FDA import refusal record(s) in our database, spanning from 6/1/2006 to 6/1/2006.

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. Whenzhou Pharmaceutical Factory (Offices)'s FEI number is 3002603232.

What types of violations has Whenzhou Pharmaceutical Factory (Offices) received?

Whenzhou Pharmaceutical Factory (Offices) has been cited for 2 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 Whenzhou Pharmaceutical Factory (Offices) come from?

All FDA import refusal data for Whenzhou Pharmaceutical Factory (Offices) 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.