Cal Pacific Corporation
⚠️ Moderate Risk
FEI: 3003942397 • Caloocan City • PHILIPPINES
FEI Number
3003942397
Location
Caloocan City
Country
PHILIPPINESAddress
1081-A Mba 1 Subd.Bagumbong, , Caloocan City, , Philippines
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
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
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.
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).
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.
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.
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.
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 |
|---|---|---|---|
| 3/23/2012 | 28AGT54PEPPER,BLACK, WHOLE (SPICE) | 9SALMONELLA | San Francisco District Office (SAN-DO) |
| 6/20/2011 | 28AGT54PEPPER,BLACK, WHOLE (SPICE) | 9SALMONELLA | San Francisco District Office (SAN-DO) |
| 10/1/2007 | 27VCP99VINEGAR, N.E.C. | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 5/15/2007 | 24TGT99LEAF & STEM VEGETABLES, N.E.C. | 9SALMONELLA | San Francisco District Office (SAN-DO) |
| 1/3/2006 | 33CGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE) | 249FILTHY | San Francisco District Office (SAN-DO) |
| 1/3/2006 | 33CGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE) | 249FILTHY | San Francisco District Office (SAN-DO) |
| 10/14/2004 | 24TGH99LEAF & STEM VEGETABLES, N.E.C. | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
| 5/6/2004 | 28AGT99WHOLE SPICE, N.E.C. | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 4/7/2004 | 20SHT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | Los Angeles District Office (LOS-DO) | |
| 4/7/2004 | 21SHT05MANGO (SUBTROPICAL AND TROPICAL FRUIT) | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Cal Pacific Corporation's FDA import refusal history?
Cal Pacific Corporation (FEI: 3003942397) has 10 FDA import refusal record(s) in our database, spanning from 4/7/2004 to 3/23/2012.
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. Cal Pacific Corporation's FEI number is 3003942397.
What types of violations has Cal Pacific Corporation received?
Cal Pacific Corporation has been cited for 7 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 Cal Pacific Corporation come from?
All FDA import refusal data for Cal Pacific Corporation 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.