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Zhejiang Cheng Yi Pharmaceutical Co., Ltd.

⚠️ Moderate Risk

FEI: 3004090742 • Wenzhou, Zhejiang • CHINA

FEI

FEI Number

3004090742

📍

Location

Wenzhou, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

118 Hua Gong Road, Dongtou District, Wenzhou, Zhejiang, China

Moderate Risk

FDA Import Risk Assessment

34.6
LowModerateHighCritical

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

Statistics

6
Total Refusals
4
Unique Violations
1/25/2016
Latest Refusal
9/13/2012
Earliest Refusal

Score Breakdown

Violation Severity
58.6×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
17.8×10%
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

1184×

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.

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.

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
1/25/2016
64TAT01AZATHIOPRINE (IMMUNOSUPPRESSIVE)
16DIRECTIONS
3280FRNMFGREG
Cincinnati District Office (CIN-DO)
4/12/2013
64TCB01AZATHIOPRINE (IMMUNOSUPPRESSIVE)
118NOT LISTED
New Orleans District Office (NOL-DO)
9/13/2012
62VCS12RIBAVIRIN (ANTI-VIRAL)
118NOT LISTED
San Juan District Office (SJN-DO)
9/13/2012
62VCC12RIBAVIRIN (ANTI-VIRAL)
118NOT LISTED
San Juan District Office (SJN-DO)
9/13/2012
62VCC12RIBAVIRIN (ANTI-VIRAL)
118NOT LISTED
San Juan District Office (SJN-DO)
9/13/2012
62VCC12RIBAVIRIN (ANTI-VIRAL)
75UNAPPROVED
San Juan District Office (SJN-DO)

Frequently Asked Questions

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

Zhejiang Cheng Yi Pharmaceutical Co., Ltd. (FEI: 3004090742) has 6 FDA import refusal record(s) in our database, spanning from 9/13/2012 to 1/25/2016.

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. Zhejiang Cheng Yi Pharmaceutical Co., Ltd.'s FEI number is 3004090742.

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

Zhejiang Cheng Yi 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 Zhejiang Cheng Yi Pharmaceutical Co., Ltd. come from?

All FDA import refusal data for Zhejiang Cheng Yi 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.