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Violation Code: 2220

FDA Violation

Charge Code: INGRED FIL

1
Total Refusals
1
Affected Firms
1/11/2022
Latest Case
1/11/2022
First Case

Violation Details

Violation Code (ASC ID)
2220
Charge Code
INGRED FIL
Description
The article appears to be an ingredient in a dietary supplement and may have been prepared packed or held under insanitary conditions whereby it may have become contaminated with filth or rendered injurious to health.
Legal Section
402(a)(4), 801(a)(3); Adulteration

Most Affected Firms

#Firm NameLocationCases
1PROCESSORS AND EXPORTERS OF HEALTH FOOD SUPPLEMENTChristchurch, NEW ZEALAN1

Recent Import Refusals

DateProductFirm
1/11/2022
ANIMAL BY-PRODUCTS AND EXTRACTS, N.E.C.
54GCH99

Related Violations

Other violations under the same legal section: 402(a)(4), 801(a)(3); Adulteration

CodeCharge CodeCases
2202INSAN BSE7

Frequently Asked Questions

What is FDA violation code 2220?

2220 is an FDA violation code that indicates: "The article appears to be an ingredient in a dietary supplement and may have been prepared packed or held under insanitary conditions whereby it may have become contaminated with filth or rendered injurious to health.". This violation is based on 402(a)(4), 801(a)(3); Adulteration of the Federal Food, Drug, and Cosmetic Act.

How many import refusals have been issued for violation 2220?

According to FDA Import Refusal data, there have been 1 import refusals issued for violation code 2220, affecting 1 unique firms.

When was the most recent refusal for violation 2220?

The most recent import refusal for violation 2220 was on January 11, 2022.

What products are commonly refused for violation 2220?

Products commonly refused under violation 2220 include: ANIMAL BY-PRODUCTS AND EXTRACTS, N.E.C.. These products were refused entry because they did not meet FDA requirements.

What is the legal basis for FDA violation code 2220?

Violation code 2220 is based on 402(a)(4), 801(a)(3); Adulteration of the Federal Food, Drug, and Cosmetic Act (FD&C Act). This section of the law establishes requirements that imported products must meet to be allowed entry into the United States.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.