FATTORIE CHIARAPPA S.R.L.
⚠️ Moderate Risk
FEI: 3004335822 • 5 Conversano, Bari • ITALY
FEI Number
3004335822
Location
5 Conversano, Bari
Country
ITALYAddress
Via Dell'Ulivo, , 5 Conversano, Bari, Italy
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
LISTERIA
The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.
Refusal History
Frequently Asked Questions
What is FATTORIE CHIARAPPA S.R.L.'s FDA import refusal history?
FATTORIE CHIARAPPA S.R.L. (FEI: 3004335822) has 2 FDA import refusal record(s) in our database, spanning from 12/17/2012 to 12/17/2012.
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. FATTORIE CHIARAPPA S.R.L.'s FEI number is 3004335822.
What types of violations has FATTORIE CHIARAPPA S.R.L. received?
FATTORIE CHIARAPPA S.R.L. 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 FATTORIE CHIARAPPA S.R.L. come from?
All FDA import refusal data for FATTORIE CHIARAPPA S.R.L. 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.