SACLA CDA
⚠️ High Risk
FEI: 3032148852 • Castello Di Annone • ITALY
FEI Number
3032148852
Location
Castello Di Annone
Country
ITALYAddress
S.P. 27 Castello Di Ann, , Castello Di Annone, , Italy
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
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).
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 |
|---|---|---|---|
| 1/22/2026 | 37JCI99SAUCES, N.E.C. | Division of Southeast Imports (DSEI) | |
| 1/22/2026 | 24VCN01ARTICHOKE, WITH SAUCE | Division of Southeast Imports (DSEI) | |
| 1/22/2026 | 37JCI25BASIL SAUCE (WITH OTHER INGREDIENTS) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is SACLA CDA's FDA import refusal history?
SACLA CDA (FEI: 3032148852) has 3 FDA import refusal record(s) in our database, spanning from 1/22/2026 to 1/22/2026.
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. SACLA CDA's FEI number is 3032148852.
What types of violations has SACLA CDA received?
SACLA CDA has been cited for 2 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 SACLA CDA come from?
All FDA import refusal data for SACLA CDA 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.