POKKA CORPORATION CO.,LTD
⚠️ Moderate Risk
FEI: 3004699151 • Nagoya • JAPAN
FEI Number
3004699151
Location
Nagoya
Country
JAPANAddress
35 16 Daiichi Fuji Bld., Aiti Daikan-Cho; Higashi, Nagoya, , 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
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.
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).
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/18/2002 | 31KGT02TEA, GREEN | Los Angeles District Office (LOS-DO) | |
| 1/18/2002 | 31KGT02TEA, GREEN | Los Angeles District Office (LOS-DO) | |
| 1/18/2002 | 31KGT02TEA, GREEN | Los Angeles District Office (LOS-DO) | |
| 1/18/2002 | 31KGT02TEA, GREEN | Los Angeles District Office (LOS-DO) | |
| 1/18/2002 | 31KGT02TEA, GREEN | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 1/18/2002 | 31AGE99COFFEE, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 1/18/2002 | 31KGT02TEA, GREEN | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is POKKA CORPORATION CO.,LTD's FDA import refusal history?
POKKA CORPORATION CO.,LTD (FEI: 3004699151) has 7 FDA import refusal record(s) in our database, spanning from 1/18/2002 to 1/18/2002.
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. POKKA CORPORATION CO.,LTD's FEI number is 3004699151.
What types of violations has POKKA CORPORATION CO.,LTD received?
POKKA CORPORATION 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 POKKA CORPORATION CO.,LTD come from?
All FDA import refusal data for POKKA CORPORATION 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.