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SINT MAARTEN

SINT MAART

FDA import refusal data for products from SINT MAARTEN

13
Total Firms
21
Total Refusals
3/3/2016
Latest Refusal

Common Violations

13

UNAPPROVED

6

NOT LISTED

2

CSTIC LBLG

1

NO ENGLISH

1

INCONSPICU

1

NON STD

1

NO ENGLISH

1

RX LEGEND

1

RX DEVICE

10218
1

LIST INGRE

Top Firms

#Firm NameRiskRefusals
1
Caraibes Sante Beaute

Marigot St Maarten

Risk: 41.46
2Risk: 31.03
3
Osner Olin

St Maarten

Risk: 43.32
4
John Davis

Simpson Bay

Risk: 40.31
5Risk: 18.31
6
Mvg Tech

Philipsburg

Risk: 32.31
7
Grand Bazaar

St Martin

Risk: 26.31
8
Natacha Carty

Simpson Bay

Risk: 40.31
9Risk: 32.31
10
Franklin Chang Sing Pang

St Maartenst Maarten

Risk: 40.31
11Risk: 40.31
12
Lucky Wholesale

Philipsburg

Risk: 36.31
13
Dudley Larocque

St Maartenst Maarten

Risk: 30.31

Frequently Asked Questions

How many FDA import refusals are from SINT MAARTEN?

According to FDA records, there have been 21 import refusals for products originating from SINT MAARTEN, involving 13 firms.

What products from SINT MAARTEN are commonly refused by the FDA?

Products from SINT MAARTEN 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 SINT MAARTEN are unsafe?

Not necessarily. An import refusal indicates a specific shipment appeared to violate FDA requirements at the time of inspection. Many SINT MAARTEN 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 SINT MAARTEN?

Our database includes FDA import refusals for SINT MAARTEN through 3/3/2016. 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.