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guangzhou p'product

⚠️ Moderate Risk

FEI: 3004319550 • Guangzhou, Guangdong • CHINA

FEI

FEI Number

3004319550

📍

Location

Guangzhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Chadong Industry Panyu, Shi Ji, Guangzhou, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

44.7
LowModerateHighCritical

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

Statistics

10
Total Refusals
8
Unique Violations
4/8/2009
Latest Refusal
7/6/2004
Earliest Refusal

Score Breakdown

Violation Severity
77.5×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
21.0×10%
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

2515×

POISONOUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:

2382×

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.

2492×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

2602×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

2182×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

2811×

BACTERIA

The article appears to contain a poisonous and deleterious substance which may render it injurious to health. Contains

3191×

WRONG IDEN

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded as defined in section 403(b) of the FD&C Act. The article appears to be offered for sale under the name of another food.

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
4/8/2009
54EDH99HERBALS & BOTANICAL TEAS, N.E.C.
218LIST INGRE
251POISONOUS
260FALSE
San Francisco District Office (SAN-DO)
11/19/2007
54EYT09EPHEDRA (HERBAL & BOTANICAL TEAS)
238UNSAFE ADD
San Francisco District Office (SAN-DO)
11/19/2007
54EYT09EPHEDRA (HERBAL & BOTANICAL TEAS)
238UNSAFE ADD
San Francisco District Office (SAN-DO)
5/15/2007
54EDH99HERBALS & BOTANICAL TEAS, N.E.C.
218LIST INGRE
251POISONOUS
260FALSE
319WRONG IDEN
San Francisco District Office (SAN-DO)
3/19/2007
54FGH16LICORICE (HERBAL & BOTANICALS, NOT TEAS)
251POISONOUS
San Francisco District Office (SAN-DO)
12/16/2005
54FBT12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
249FILTHY
320LACKS FIRM
San Francisco District Office (SAN-DO)
9/3/2004
54EDH99HERBALS & BOTANICAL TEAS, N.E.C.
281BACTERIA
San Francisco District Office (SAN-DO)
9/3/2004
54EDH99HERBALS & BOTANICAL TEAS, N.E.C.
251POISONOUS
San Francisco District Office (SAN-DO)
9/3/2004
21HGH16CHINESE RED DATE (JUJUBES, ZIZIPHUS JUJUBA), DRIED OR PASTE
249FILTHY
San Francisco District Office (SAN-DO)
7/6/2004
28AGH19GINGER, WHOLE (SPICE)
251POISONOUS
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is guangzhou p'product's FDA import refusal history?

guangzhou p'product (FEI: 3004319550) has 10 FDA import refusal record(s) in our database, spanning from 7/6/2004 to 4/8/2009.

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. guangzhou p'product's FEI number is 3004319550.

What types of violations has guangzhou p'product received?

guangzhou p'product has been cited for 8 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 guangzhou p'product come from?

All FDA import refusal data for guangzhou p'product 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.