Iris Granville
⚠️ Moderate Risk
FEI: 3009821964 • Kumasi • GHANA
FEI Number
3009821964
Location
Kumasi
Country
GHANAAddress
Ma 16, Manhiya Ashanti, , Kumasi, , Ghana
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
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.
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
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.
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.
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/20/2012 | 25JFY99ROOT & TUBER VEGETABLE, N.E.C. | Florida District Office (FLA-DO) | |
| 12/20/2012 | 16VFY14SNAILS, AQUATIC COLD SMOKED, OTHER AQUATIC SPECIES | Florida District Office (FLA-DO) | |
| 12/20/2012 | 23YFY99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C. | Florida District Office (FLA-DO) | |
| 12/20/2012 | 16IFH99FISH, HOT SMOKED N.E.C. | Florida District Office (FLA-DO) | |
| 12/20/2012 | 25JFY12SWEET POTATO (ROOT & TUBER VEGETABLE) | Florida District Office (FLA-DO) | |
| 12/20/2012 | 23OFY07PEANUT, NUT FLOUR/MEAL | Florida District Office (FLA-DO) | |
| 12/20/2012 | 28BFY24MACE, GROUND, CRACKED (SPICE) | Florida District Office (FLA-DO) | |
| 12/20/2012 | 25LFY16CASSAVA, DRIED OR PASTE | Florida District Office (FLA-DO) | |
| 12/20/2012 | 16XFY21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS | Florida District Office (FLA-DO) | |
| 12/20/2012 | 16AYH99FISH, N.E.C. | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Iris Granville's FDA import refusal history?
Iris Granville (FEI: 3009821964) has 10 FDA import refusal record(s) in our database, spanning from 12/20/2012 to 12/20/2012.
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. Iris Granville's FEI number is 3009821964.
What types of violations has Iris Granville received?
Iris Granville has been cited for 6 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 Iris Granville come from?
All FDA import refusal data for Iris Granville 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.