Pac Company Limited
✅ Low Risk
FEI: 3004505328 • Guangdong • CHINA
FEI Number
3004505328
Location
Guangdong
Country
CHINAAddress
344 Dong Jiang Rd, , Guangdong, , China
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/10/2005 | 33LGY99SOFT CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE) | 274COLOR LBLG | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Pac Company Limited's FDA import refusal history?
Pac Company Limited (FEI: 3004505328) has 1 FDA import refusal record(s) in our database, spanning from 8/10/2005 to 8/10/2005.
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. Pac Company Limited's FEI number is 3004505328.
What types of violations has Pac Company Limited received?
Pac Company Limited has been cited for 1 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 Pac Company Limited come from?
All FDA import refusal data for Pac Company 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.