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Pleasure Chest Group Company Ltd

⚠️ Moderate Risk

FEI: 3008984859 • Zhejiang • CHINA

FEI

FEI Number

3008984859

📍

Location

Zhejiang

🇨🇳

Country

CHINA
🏢

Address

Add F6 No.777 North Chouzhou Rd, , Zhejiang, , China

Moderate Risk

FDA Import Risk Assessment

25.8
LowModerateHighCritical

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

Statistics

2
Total Refusals
7
Unique Violations
8/26/2011
Latest Refusal
8/19/2011
Earliest Refusal

Score Breakdown

Violation Severity
46.3×40%
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

3412×

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).

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.

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

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).

4771×

HOLES

The quality of the article falls below that which it purports or is represented to possess, in that the devices contain defects/holes.

5081×

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.

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.

Refusal History

DateProductViolationsDivision
8/26/2011
85HISCONDOM
16DIRECTIONS
3260NO ENGLISH
333LACKS FIRM
341REGISTERED
477HOLES
Southwest Import District Office (SWI-DO)
8/19/2011
85KXQVIBRATOR FOR THERAPEUTIC USE, GENITAL
118NOT LISTED
341REGISTERED
508NO 510(K)
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Pleasure Chest Group Company Ltd's FDA import refusal history?

Pleasure Chest Group Company Ltd (FEI: 3008984859) has 2 FDA import refusal record(s) in our database, spanning from 8/19/2011 to 8/26/2011.

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. Pleasure Chest Group Company Ltd's FEI number is 3008984859.

What types of violations has Pleasure Chest Group Company Ltd received?

Pleasure Chest Group Company Ltd has been cited for 7 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 Pleasure Chest Group Company Ltd come from?

All FDA import refusal data for Pleasure Chest Group Company 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.