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SHENZHEN HIGHTOP BIOTECH CO., LT

⚠️ Moderate Risk

FEI: 3036568145 • Guangdong • CHINA

FEI

FEI Number

3036568145

📍

Location

Guangdong

🇨🇳

Country

CHINA
🏢

Address

902, 9/F, Block A, Maoy, , Guangdong, , China

Moderate Risk

FDA Import Risk Assessment

44.0
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
5/7/2025
Latest Refusal
5/2/2025
Earliest Refusal

Score Breakdown

Violation Severity
56.0×40%
Refusal Volume
17.7×30%
Recency
71.3×20%
Frequency
20.0×10%
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

1182×

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).

32802×

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.

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

Refusal History

DateProductViolationsDivision
5/7/2025
83QYTOVER-THE-COUNTER COVID-19 ANTIGEN TEST
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
5/2/2025
83QLWCOVID-19 TEST HOME COLLECTION KIT DEVICES
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SHENZHEN HIGHTOP BIOTECH CO., LT's FDA import refusal history?

SHENZHEN HIGHTOP BIOTECH CO., LT (FEI: 3036568145) has 2 FDA import refusal record(s) in our database, spanning from 5/2/2025 to 5/7/2025.

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. SHENZHEN HIGHTOP BIOTECH CO., LT's FEI number is 3036568145.

What types of violations has SHENZHEN HIGHTOP BIOTECH CO., LT received?

SHENZHEN HIGHTOP BIOTECH CO., LT has been cited for 3 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 SHENZHEN HIGHTOP BIOTECH CO., LT come from?

All FDA import refusal data for SHENZHEN HIGHTOP BIOTECH CO., LT 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.