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Violation Code: 332

FDA Violation

Charge Code: CONTAINER

2
Total Refusals
2
Affected Firms
3/26/2020
Latest Case
8/18/2010
First Case

Violation Details

Violation Code (ASC ID)
332
Charge Code
CONTAINER
Description
The container appears to be composed, in whole or in part, of a poisonous or deleterious substance which may render the contents injurious to health.
Legal Section
501(a)(3), 801(a)(3); ADULTERATION

Most Affected Firms

#Firm NameLocationCases
1Veranova LPWest Deptford, UNITED STA1
2Mesoestetic S.L.Viladecans, SPAIN1

Recent Import Refusals

DateProductFirm
3/26/2020
CARBOPLATIN (ANTI-NEOPLASTIC - PART II)
62ZAS01
Veranova LPUNITED STA
8/18/2010
CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS)
53LC01

Frequently Asked Questions

What is FDA violation code 332?

332 is an FDA violation code that indicates: "The container appears to be composed, in whole or in part, of a poisonous or deleterious substance which may render the contents injurious to health.". This violation is based on 501(a)(3), 801(a)(3); ADULTERATION of the Federal Food, Drug, and Cosmetic Act.

How many import refusals have been issued for violation 332?

According to FDA Import Refusal data, there have been 2 import refusals issued for violation code 332, affecting 2 unique firms.

When was the most recent refusal for violation 332?

The most recent import refusal for violation 332 was on March 26, 2020.

What products are commonly refused for violation 332?

Products commonly refused under violation 332 include: CARBOPLATIN (ANTI-NEOPLASTIC - PART II), CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS). These products were refused entry because they did not meet FDA requirements.

What is the legal basis for FDA violation code 332?

Violation code 332 is based on 501(a)(3), 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.