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MIU LAB

Low Risk

FEI: 3013612295 • ZHEJIANG • CHINA

FEI

FEI Number

3013612295

📍

Location

ZHEJIANG

🇨🇳

Country

CHINA
🏢

Address

2F BLOCK 1 DEYU BLDG 14, , ZHEJIANG, , China

Low Risk

FDA Import Risk Assessment

20.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
6
Unique Violations
8/8/2017
Latest Refusal
8/8/2017
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
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

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).

2781×

NO TAG

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product to which is not affixed a certification in the form of a label or tag in conformity with section 534(h).

2881×

STD LABEL

The article appears to not bear labeling prescribed by the performance standard established under section 514.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

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).

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
8/8/2017
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
278NO TAG
288STD LABEL
333LACKS FIRM
341REGISTERED
476NO REGISTR
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MIU LAB's FDA import refusal history?

MIU LAB (FEI: 3013612295) has 1 FDA import refusal record(s) in our database, spanning from 8/8/2017 to 8/8/2017.

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. MIU LAB's FEI number is 3013612295.

What types of violations has MIU LAB received?

MIU LAB has been cited for 6 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 MIU LAB come from?

All FDA import refusal data for MIU LAB 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.