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Asia Pacific Perfect Technology Co Ltd

⚠️ Moderate Risk

FEI: 3016195089 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3016195089

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Floor 3 , No.13 , 1st Daxing Road , Buyong Community Floor 2, Shajing Main Street; Baoan, Shenzhen, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

31.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
8/20/2020
Latest Refusal
4/22/2020
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
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

5082×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

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).

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
8/20/2020
80FLLTHERMOMETER, ELECTRONIC, CLINICAL
508NO 510(K)
Division of Southeast Imports (DSEI)
4/22/2020
80PXHTHERMOMETER KIT
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Asia Pacific Perfect Technology Co Ltd's FDA import refusal history?

Asia Pacific Perfect Technology Co Ltd (FEI: 3016195089) has 2 FDA import refusal record(s) in our database, spanning from 4/22/2020 to 8/20/2020.

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. Asia Pacific Perfect Technology Co Ltd's FEI number is 3016195089.

What types of violations has Asia Pacific Perfect Technology Co Ltd received?

Asia Pacific Perfect Technology Co Ltd 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 Asia Pacific Perfect Technology Co Ltd come from?

All FDA import refusal data for Asia Pacific Perfect Technology 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.