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Andon Health Co., Ltd.

⚠️ Moderate Risk

FEI: 3008177000 • Tianjin, Tianjin • CHINA

FEI

FEI Number

3008177000

📍

Location

Tianjin, Tianjin

🇨🇳

Country

CHINA
🏢

Address

Jinpinglu, , Tianjin, Tianjin, China

Moderate Risk

FDA Import Risk Assessment

28.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
5/20/2016
Latest Refusal
10/4/2011
Earliest Refusal

Score Breakdown

Violation Severity
53.3×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
6.5×10%
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

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).

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).

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

Refusal History

DateProductViolationsDivision
5/20/2016
75NBWSYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER
118NOT LISTED
Seattle District Office (SEA-DO)
2/19/2014
74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
341REGISTERED
Cincinnati District Office (CIN-DO)
10/4/2011
75NBWSYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER
237NO PMA
New York District Office (NYK-DO)

Frequently Asked Questions

What is Andon Health Co., Ltd.'s FDA import refusal history?

Andon Health Co., Ltd. (FEI: 3008177000) has 3 FDA import refusal record(s) in our database, spanning from 10/4/2011 to 5/20/2016.

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. Andon Health Co., Ltd.'s FEI number is 3008177000.

What types of violations has Andon Health Co., Ltd. received?

Andon Health 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 Andon Health Co., Ltd. come from?

All FDA import refusal data for Andon Health 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.