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Masson Group

⚠️ Moderate Risk

FEI: 3005246994 • Guangzhou, Guang Dong • TAIWAN

FEI

FEI Number

3005246994

📍

Location

Guangzhou, Guang Dong

🇹🇼

Country

TAIWAN
🏢

Address

No. 48 Shamian South, , Li Wan, Guangzhou, Guang Dong, Taiwan

Moderate Risk

FDA Import Risk Assessment

27.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
6
Unique Violations
7/26/2005
Latest Refusal
7/26/2005
Earliest Refusal

Score Breakdown

Violation Severity
58.3×40%
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

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

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.

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

3441×

WARNINGS

It appears to lack adequate warning against use in a pathological condition or by children where it may be dangerous to health or against an unsafe dose, method, administering duration, application, in manner/form, to protect users.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
7/26/2005
63RBJ05SODIUM MONOFLUOROPHOSPHATE (DENTAL CARIES PROPHYLACTIC)
16DIRECTIONS
333LACKS FIRM
336INCONSPICU
344WARNINGS
473LABELING
75UNAPPROVED
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Masson Group's FDA import refusal history?

Masson Group (FEI: 3005246994) has 1 FDA import refusal record(s) in our database, spanning from 7/26/2005 to 7/26/2005.

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. Masson Group's FEI number is 3005246994.

What types of violations has Masson Group received?

Masson Group 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 Masson Group come from?

All FDA import refusal data for Masson Group 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.