CAPE VERDE
CAPE VERDE
FDA import refusal data for products from CAPE VERDE
Top Firms
| # | Firm Name | Risk | Refusals |
|---|---|---|---|
| 1 | Frescomar, SA Mindelo | Risk: 43.3 | 6 |
| 2 | Risk: 36.7 | 3 | |
| 3 | Risk: 50.7 | 1 |
Frequently Asked Questions
How many FDA import refusals are from CAPE VERDE?
According to FDA records, there have been 10 import refusals for products originating from CAPE VERDE, involving 3 firms.
What products from CAPE VERDE are commonly refused by the FDA?
Products from CAPE VERDE may be refused for various reasons including adulteration, misbranding, lack of proper registration, or failure to meet U.S. safety standards. The specific products vary by firm and time period. View the common violations section on this page for more details.
Does an import refusal mean products from CAPE VERDE are unsafe?
Not necessarily. An import refusal indicates a specific shipment appeared to violate FDA requirements at the time of inspection. Many CAPE VERDE firms successfully import products that meet all FDA requirements. Import refusals help identify and prevent non-compliant products from entering the U.S. market.
How current is the FDA import refusal data for CAPE VERDE?
Our database includes FDA import refusals for CAPE VERDE through 8/8/2022. Data is sourced from the FDA Data Dashboard and updated monthly.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.