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Pharmaron (Ningbo) Technology Development Co., Ltd.

⚠️ Moderate Risk

FEI: 3013653223 • Ningbo, Zhejiang • CHINA

FEI

FEI Number

3013653223

📍

Location

Ningbo, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

Hangzhou Bay, 800 Binhai 4th Road; New Zone, Ningbo, Zhejiang, China

Moderate Risk

FDA Import Risk Assessment

49.8
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
5/30/2023
Latest Refusal
5/30/2023
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
11.2×30%
Recency
47.0×20%
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

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
5/30/2023
62VIS99ANTI-VIRAL N.E.C.
75UNAPPROVED
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is Pharmaron (Ningbo) Technology Development Co., Ltd.'s FDA import refusal history?

Pharmaron (Ningbo) Technology Development Co., Ltd. (FEI: 3013653223) has 1 FDA import refusal record(s) in our database, spanning from 5/30/2023 to 5/30/2023.

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. Pharmaron (Ningbo) Technology Development Co., Ltd.'s FEI number is 3013653223.

What types of violations has Pharmaron (Ningbo) Technology Development Co., Ltd. received?

Pharmaron (Ningbo) Technology Development 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 Pharmaron (Ningbo) Technology Development Co., Ltd. come from?

All FDA import refusal data for Pharmaron (Ningbo) Technology Development 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.