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GUANGDONG CANNERY

⚠️ Moderate Risk

FEI: 3010436857 • Guangzhou, Guangdong • CHINA

FEI

FEI Number

3010436857

📍

Location

Guangzhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Tower B. Room 1901-1905, No. 100 Xi, Guangzhou, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

45.9
LowModerateHighCritical

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

Statistics

7
Total Refusals
4
Unique Violations
5/23/2013
Latest Refusal
12/13/2010
Earliest Refusal

Score Breakdown

Violation Severity
82.5×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
28.6×10%
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

28605×

VETDRUGRES

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a new animal drug (or conversion product thereof) that is unsafe within the meaning of Section 512. Product contains

2383×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

622×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

832×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
5/23/2013
16AET57DACE
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
5/10/2013
16AEE57DACE
238UNSAFE ADD
2860VETDRUGRES
New York District Office (NYK-DO)
5/10/2013
16AEE57DACE
238UNSAFE ADD
2860VETDRUGRES
New York District Office (NYK-DO)
1/15/2013
16AET57DACE
238UNSAFE ADD
2860VETDRUGRES
New York District Office (NYK-DO)
4/17/2012
16AEE57DACE
2860VETDRUGRES
Division of Northeast Imports (DNEI)
9/20/2011
30YET01GRASS JELLY DRINK BEVERAGE BASE
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
12/13/2010
16AEE57DACE
2860VETDRUGRES
New York District Office (NYK-DO)

Frequently Asked Questions

What is GUANGDONG CANNERY's FDA import refusal history?

GUANGDONG CANNERY (FEI: 3010436857) has 7 FDA import refusal record(s) in our database, spanning from 12/13/2010 to 5/23/2013.

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. GUANGDONG CANNERY's FEI number is 3010436857.

What types of violations has GUANGDONG CANNERY received?

GUANGDONG CANNERY 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 GUANGDONG CANNERY come from?

All FDA import refusal data for GUANGDONG CANNERY 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.