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Nanhai Beisha Pharmaceutical Co., Ltd.

✅ Low Risk

FEI: 3003857764 • Foshan, Guangdong • CHINA

FEI

FEI Number

3003857764

📍

Location

Foshan, Guangdong

🇨🇳

Country

CHINA
🏢

Address

No. 21, Shaluo Industrial Zone, Beisha Village, Lishui Town, Nanhai, Foshan, Guangdong, 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
9/8/2015
Latest Refusal
9/8/2015
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

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.

Refusal History

DateProductViolationsDivision
9/8/2015
61GCT47SULFADIAZINE (ANTI-BACTERIAL) (NOT ANTIBIOTIC)
3280FRNMFGREG
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Nanhai Beisha Pharmaceutical Co., Ltd.'s FDA import refusal history?

Nanhai Beisha Pharmaceutical Co., Ltd. (FEI: 3003857764) has 1 FDA import refusal record(s) in our database, spanning from 9/8/2015 to 9/8/2015.

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. Nanhai Beisha Pharmaceutical Co., Ltd.'s FEI number is 3003857764.

What types of violations has Nanhai Beisha Pharmaceutical Co., Ltd. received?

Nanhai Beisha 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 Nanhai Beisha Pharmaceutical Co., Ltd. come from?

All FDA import refusal data for Nanhai Beisha 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.