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Lovetoys Industrial Co Ltd

⚠️ Moderate Risk

FEI: 3011061555 • Nancheng • CHINA

FEI

FEI Number

3011061555

📍

Location

Nancheng

🇨🇳

Country

CHINA
🏢

Address

Block B, Hung Tu Rd; Dongguan, Nancheng, , China

Moderate Risk

FDA Import Risk Assessment

39.9
LowModerateHighCritical

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

Statistics

15
Total Refusals
7
Unique Violations
6/30/2017
Latest Refusal
1/28/2015
Earliest Refusal

Score Breakdown

Violation Severity
50.9×40%
Refusal Volume
44.6×30%
Recency
0.0×20%
Frequency
61.9×10%
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

11815×

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).

1615×

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.

32809×

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.

5089×

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.

3338×

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.

3418×

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).

32601×

NO ENGLISH

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

Refusal History

DateProductViolationsDivision
6/30/2017
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
9/12/2016
89LYGMASSAGER, THERAPEUTIC, MANUAL
118NOT LISTED
16DIRECTIONS
Division of Southwest Imports (DSWI)
9/12/2016
89LYGMASSAGER, THERAPEUTIC, MANUAL
118NOT LISTED
16DIRECTIONS
Division of Southwest Imports (DSWI)
9/12/2016
89LYGMASSAGER, THERAPEUTIC, MANUAL
118NOT LISTED
16DIRECTIONS
Division of Southwest Imports (DSWI)
9/12/2016
89LYGMASSAGER, THERAPEUTIC, MANUAL
118NOT LISTED
16DIRECTIONS
Division of Southwest Imports (DSWI)
9/12/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
Division of Southwest Imports (DSWI)
9/12/2016
89LYGMASSAGER, THERAPEUTIC, MANUAL
118NOT LISTED
16DIRECTIONS
Division of Southwest Imports (DSWI)
1/28/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
508NO 510(K)
Baltimore District Office (BLT-DO)
1/28/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
508NO 510(K)
Baltimore District Office (BLT-DO)
1/28/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
508NO 510(K)
Baltimore District Office (BLT-DO)
1/28/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
508NO 510(K)
Baltimore District Office (BLT-DO)
1/28/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
508NO 510(K)
Baltimore District Office (BLT-DO)
1/28/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
508NO 510(K)
Baltimore District Office (BLT-DO)
1/28/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
508NO 510(K)
Baltimore District Office (BLT-DO)
1/28/2015
85HISCONDOM
118NOT LISTED
16DIRECTIONS
3260NO ENGLISH
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
508NO 510(K)
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Lovetoys Industrial Co Ltd's FDA import refusal history?

Lovetoys Industrial Co Ltd (FEI: 3011061555) has 15 FDA import refusal record(s) in our database, spanning from 1/28/2015 to 6/30/2017.

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. Lovetoys Industrial Co Ltd's FEI number is 3011061555.

What types of violations has Lovetoys Industrial Co Ltd received?

Lovetoys Industrial Co 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 Lovetoys Industrial Co Ltd come from?

All FDA import refusal data for Lovetoys Industrial 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.