Shikoku Meiji Inryo Co., Ltd
⚠️ Moderate Risk
FEI: 1000344848 • Takamatsu, Kagawa • JAPAN
FEI Number
1000344848
Location
Takamatsu, Kagawa
Country
JAPANAddress
785-4, Kanotsuno-Cho, Takamatsu, Kagawa, Japan
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
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).
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.
PRESRV LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/8/2016 | 29AHE99NONCARBONATED SOFT DRINK, N.E.C. | Seattle District Office (SEA-DO) | |
| 2/8/2016 | 29AHE99NONCARBONATED SOFT DRINK, N.E.C. | Seattle District Office (SEA-DO) | |
| 2/8/2016 | 29AHE99NONCARBONATED SOFT DRINK, N.E.C. | Seattle District Office (SEA-DO) | |
| 7/29/2005 | 30BHT06BEVERAGE BASE, SUBTROPICAL OR TROPICAL FRUIT, LIQUID | San Francisco District Office (SAN-DO) | |
| 7/6/2005 | 30KHT07BEVERAGE BASE, IMITATION VINE FRUIT, LIQUID | 11UNSAFE COL | Los Angeles District Office (LOS-DO) |
| 8/29/2003 | 29AGT99NONCARBONATED SOFT DRINK, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Shikoku Meiji Inryo Co., Ltd's FDA import refusal history?
Shikoku Meiji Inryo Co., Ltd (FEI: 1000344848) has 6 FDA import refusal record(s) in our database, spanning from 8/29/2003 to 2/8/2016.
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. Shikoku Meiji Inryo Co., Ltd's FEI number is 1000344848.
What types of violations has Shikoku Meiji Inryo Co., Ltd received?
Shikoku Meiji Inryo 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 Shikoku Meiji Inryo Co., Ltd come from?
All FDA import refusal data for Shikoku Meiji Inryo 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.