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Wenzhou Dongwu Optical Instrument Co., Ltd.

⚠️ Moderate Risk

FEI: 3005515335 • Wenzhou, Zhejiang • CHINA

FEI

FEI Number

3005515335

📍

Location

Wenzhou, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

NO. 47 Lane 3, Woqitu, Shuangyu, Wenzhou, Zhejiang, China

Moderate Risk

FDA Import Risk Assessment

29.4
LowModerateHighCritical

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

Statistics

10
Total Refusals
4
Unique Violations
6/6/2016
Latest Refusal
1/28/2011
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
18.7×10%
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

11810×

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).

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.

32807×

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.

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).

Refusal History

DateProductViolationsDivision
6/6/2016
86HKWPRISM, BAR, OPHTHALMIC
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
Division of Southwest Imports (DSWI)
6/6/2016
86HKNREFRACTOR, MANUAL, NON-POWERED, INCLUDING PHOROPTER
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
Division of Southwest Imports (DSWI)
6/6/2016
86HKOREFRACTOMETER, OPHTHALMIC
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
Division of Southwest Imports (DSWI)
6/6/2016
86HJOBIOMICROSCOPE, SLIT-LAMP, AC-POWERED
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
Division of Southwest Imports (DSWI)
6/6/2016
86HLJOPHTHALMOSCOPE, BATTERY-POWERED
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
Division of Southwest Imports (DSWI)
6/6/2016
86HLHPUPILLOMETER, MANUAL
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
Division of Southwest Imports (DSWI)
6/6/2016
86HLMINSTRUMENT, MEASURING, LENS, AC-POWERED
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
Division of Southwest Imports (DSWI)
6/6/2016
86HLJOPHTHALMOSCOPE, BATTERY-POWERED
118NOT LISTED
333LACKS FIRM
Southwest Import District Office (SWI-DO)
1/20/2012
80FLGCLEANER, ULTRASONIC, MEDICAL INSTRUMENT
118NOT LISTED
Seattle District Office (SEA-DO)
1/28/2011
86HKNREFRACTOR, MANUAL, NON-POWERED, INCLUDING PHOROPTER
118NOT LISTED
341REGISTERED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Wenzhou Dongwu Optical Instrument Co., Ltd.'s FDA import refusal history?

Wenzhou Dongwu Optical Instrument Co., Ltd. (FEI: 3005515335) has 10 FDA import refusal record(s) in our database, spanning from 1/28/2011 to 6/6/2016.

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. Wenzhou Dongwu Optical Instrument Co., Ltd.'s FEI number is 3005515335.

What types of violations has Wenzhou Dongwu Optical Instrument Co., Ltd. received?

Wenzhou Dongwu Optical Instrument 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 Wenzhou Dongwu Optical Instrument Co., Ltd. come from?

All FDA import refusal data for Wenzhou Dongwu Optical Instrument 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.