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Dong-A Pharmaceutical Co., Ltd.

⚠️ Moderate Risk

FEI: 3010418793 • Dongdaemun, Seoul • SOUTH KOREA

FEI

FEI Number

3010418793

📍

Location

Dongdaemun, Seoul

🇰🇷
🏢

Address

Dongdaemun, 64 Cheonhodae-Ro, Dongdaemun, Seoul, South Korea

Moderate Risk

FDA Import Risk Assessment

38.5
LowModerateHighCritical

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

Statistics

10
Total Refusals
4
Unique Violations
9/20/2019
Latest Refusal
9/15/2004
Earliest Refusal

Score Breakdown

Violation Severity
65.7×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
6.7×10%
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

1188×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

754×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
9/20/2019
64BCA25HYDROCHLOROTHIAZIDE (DIURETIC)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/28/2012
60LDL01ACETAMINOPHEN (ANALGESIC)
118NOT LISTED
Atlanta District Office (ATL-DO)
3/19/2008
29ACT99NONCARBONATED SOFT DRINK, N.E.C.
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
1/3/2006
63RBY04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
Los Angeles District Office (LOS-DO)
1/3/2006
63RBY04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
Los Angeles District Office (LOS-DO)
12/27/2005
63RBY04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
Los Angeles District Office (LOS-DO)
12/27/2005
63RBY04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
Los Angeles District Office (LOS-DO)
10/5/2005
63RBY05SODIUM MONOFLUOROPHOSPHATE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
75UNAPPROVED
Seattle District Office (SEA-DO)
10/5/2005
63RBY05SODIUM MONOFLUOROPHOSPHATE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
75UNAPPROVED
Seattle District Office (SEA-DO)
9/15/2004
60SCC99ANTACID, N.E.C.
75UNAPPROVED
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Dong-A Pharmaceutical Co., Ltd.'s FDA import refusal history?

Dong-A Pharmaceutical Co., Ltd. (FEI: 3010418793) has 10 FDA import refusal record(s) in our database, spanning from 9/15/2004 to 9/20/2019.

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. Dong-A Pharmaceutical Co., Ltd.'s FEI number is 3010418793.

What types of violations has Dong-A Pharmaceutical Co., Ltd. received?

Dong-A Pharmaceutical Co., Ltd. has been cited for 4 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 Dong-A Pharmaceutical Co., Ltd. come from?

All FDA import refusal data for Dong-A Pharmaceutical Co., Ltd. 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.