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Zhejiang Changming Pharmaceutical Co., Ltd.

✅ Low Risk

FEI: 3006712427 • Taizhou, Zhejiang • CHINA

FEI

FEI Number

3006712427

📍

Location

Taizhou, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

No. 1 Badu Road, Tiantai Industrial Park, Chicheng Street, Tiantai, Taizhou, Zhejiang, China

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
1
Unique Violations
7/25/2013
Latest Refusal
7/25/2013
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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).

Refusal History

DateProductViolationsDivision
7/25/2013
62CCS99ANTI-HYPERTENSIVE N.E.C.
118NOT LISTED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Zhejiang Changming Pharmaceutical Co., Ltd.'s FDA import refusal history?

Zhejiang Changming Pharmaceutical Co., Ltd. (FEI: 3006712427) has 1 FDA import refusal record(s) in our database, spanning from 7/25/2013 to 7/25/2013.

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. Zhejiang Changming Pharmaceutical Co., Ltd.'s FEI number is 3006712427.

What types of violations has Zhejiang Changming Pharmaceutical Co., Ltd. received?

Zhejiang Changming Pharmaceutical Co., Ltd. has been cited for 1 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 Zhejiang Changming Pharmaceutical Co., Ltd. come from?

All FDA import refusal data for Zhejiang Changming 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.