ImportRefusal LogoImportRefusal

Grayco Sales Limited

⚠️ Moderate Risk

FEI: 3000164638 • Richmond Hill, Ontario • CANADA

FEI

FEI Number

3000164638

📍

Location

Richmond Hill, Ontario

🇨🇦

Country

CANADA
🏢

Address

Suite 56, 40 Vogell Rd, Richmond Hill, Ontario, Canada

Moderate Risk

FDA Import Risk Assessment

30.6
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
8/24/2009
Latest Refusal
7/26/2004
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
7.9×10%
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

2184×

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.

112×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

3062×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

3212×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

4822×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

Refusal History

DateProductViolationsDivision
8/24/2009
02DGT03RICE, ENRICHED PROCESSED (PACKAGED)
218LIST INGRE
New York District Office (NYK-DO)
8/24/2009
02DGT03RICE, ENRICHED PROCESSED (PACKAGED)
218LIST INGRE
New York District Office (NYK-DO)
7/26/2004
20KMT99CITRUS FRUIT, N.E.C., CITRUS FRUIT JUICES OR CONCENTRATES
11UNSAFE COL
218LIST INGRE
306INSANITARY
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
7/26/2004
20KMT99CITRUS FRUIT, N.E.C., CITRUS FRUIT JUICES OR CONCENTRATES
11UNSAFE COL
218LIST INGRE
306INSANITARY
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is Grayco Sales Limited's FDA import refusal history?

Grayco Sales Limited (FEI: 3000164638) has 4 FDA import refusal record(s) in our database, spanning from 7/26/2004 to 8/24/2009.

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. Grayco Sales Limited's FEI number is 3000164638.

What types of violations has Grayco Sales Limited received?

Grayco Sales Limited has been cited for 5 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 Grayco Sales Limited come from?

All FDA import refusal data for Grayco Sales Limited 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.