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Nanma Manufacturing Co.,Ltd.

⚠️ Moderate Risk

FEI: 3005162971 • Chai Wan, Hong Kong Island • HONG KONG

FEI

FEI Number

3005162971

📍

Location

Chai Wan, Hong Kong Island

🇭🇰

Country

HONG KONG
🏢

Address

Chai Wan Industrial City Block 1, 60 Wing Tai Road, Chai Wan, Hong Kong Island, Hong Kong

Moderate Risk

FDA Import Risk Assessment

35.6
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
5/10/2016
Latest Refusal
4/24/2015
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
38.2×10%
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

1184×

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).

5084×

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.

163×

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.

32803×

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.

Refusal History

DateProductViolationsDivision
5/10/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
5/5/2016
78PIAVIBRATOR FOR CLIMAX CONTROL OF PREMATURE EJACULATION
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
3/24/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
4/24/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Nanma Manufacturing Co.,Ltd.'s FDA import refusal history?

Nanma Manufacturing Co.,Ltd. (FEI: 3005162971) has 4 FDA import refusal record(s) in our database, spanning from 4/24/2015 to 5/10/2016.

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. Nanma Manufacturing Co.,Ltd.'s FEI number is 3005162971.

What types of violations has Nanma Manufacturing Co.,Ltd. received?

Nanma Manufacturing Co.,Ltd. has been cited for 4 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 Nanma Manufacturing Co.,Ltd. come from?

All FDA import refusal data for Nanma Manufacturing 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.