ImportRefusal LogoImportRefusal

AT BIO

⚠️ Moderate Risk

FEI: 3014223586 • Pocheon, Gyeonggi • SOUTH KOREA

FEI

FEI Number

3014223586

📍

Location

Pocheon, Gyeonggi

🇰🇷
🏢

Address

54-3 Orimpo-Gil, Naechon-Myeon, Pocheon, Gyeonggi, South Korea

Moderate Risk

FDA Import Risk Assessment

39.8
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

11
Total Refusals
8
Unique Violations
3/6/2020
Latest Refusal
3/6/2020
Earliest Refusal

Score Breakdown

Violation Severity
44.5×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
100.0×10%
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

3246×

NO ENGLISH

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

3215×

LACKS N/C

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

2604×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

112×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2742×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

22801×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

36021×

DR PACKGNG

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to be a drug and its container is so made, formed, or filled as to be misleading

721×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

Refusal History

DateProductViolationsDivision
3/6/2020
66VRY99MISCELLANEOUS PATENT MEDICINES, ETC.
2280DIRSEXMPT
3602DR PACKGNG
72NEW VET DR
Division of West Coast Imports (DWCI)
3/6/2020
72GYT02POULTRY PRODUCTS, PET TREATS
324NO ENGLISH
Division of West Coast Imports (DWCI)
3/6/2020
72GYT05COMBINATION PRODUCTS, PET TREATS
324NO ENGLISH
Division of West Coast Imports (DWCI)
3/6/2020
72GYT05COMBINATION PRODUCTS, PET TREATS
324NO ENGLISH
Division of West Coast Imports (DWCI)
3/6/2020
72GYT02POULTRY PRODUCTS, PET TREATS
324NO ENGLISH
Division of West Coast Imports (DWCI)
3/6/2020
72BYT05COMB PROD PET DOG FOOD
260FALSE
321LACKS N/C
Division of West Coast Imports (DWCI)
3/6/2020
72BYT05COMB PROD PET DOG FOOD
260FALSE
321LACKS N/C
Division of West Coast Imports (DWCI)
3/6/2020
72BYT05COMB PROD PET DOG FOOD
260FALSE
321LACKS N/C
Division of West Coast Imports (DWCI)
3/6/2020
72BYT05COMB PROD PET DOG FOOD
260FALSE
Division of West Coast Imports (DWCI)
3/6/2020
72GGT03FISH-SEAFOOD PRODUCTS. PET TREATS
11UNSAFE COL
274COLOR LBLG
321LACKS N/C
324NO ENGLISH
Division of West Coast Imports (DWCI)
3/6/2020
72GYT99PET TREATS, N.E.C.
11UNSAFE COL
274COLOR LBLG
321LACKS N/C
324NO ENGLISH
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is AT BIO's FDA import refusal history?

AT BIO (FEI: 3014223586) has 11 FDA import refusal record(s) in our database, spanning from 3/6/2020 to 3/6/2020.

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. AT BIO's FEI number is 3014223586.

What types of violations has AT BIO received?

AT BIO has been cited for 8 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 AT BIO come from?

All FDA import refusal data for AT BIO 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.