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Min Tong Pharmaceutical Company

⚠️ Moderate Risk

FEI: 3003572561 • Taichung • TAIWAN

FEI

FEI Number

3003572561

📍

Location

Taichung

🇹🇼

Country

TAIWAN
🏢

Address

Factory 15, 21 St Road, Industrial Zone, , Taichung, , Taiwan

Moderate Risk

FDA Import Risk Assessment

46.2
LowModerateHighCritical

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

Statistics

20
Total Refusals
8
Unique Violations
9/29/2016
Latest Refusal
2/28/2002
Earliest Refusal

Score Breakdown

Violation Severity
75.4×40%
Refusal Volume
49.0×30%
Recency
0.0×20%
Frequency
13.7×10%
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

2519×

POISONOUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:

24606×

UNSFDIETLB

The article appears to be a dietary supplement or contain a dietary ingredient that presents a significant or unreasonable risk of illness or injury under the conditions of use set out in the labeling or, if none are set out in the labeling, under customary conditions of use.

4823×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

31402×

SBGINSENG

The article is subject to refusal of admission in that it appears to be Misbranded because it or its ingredients purport to be or are represented as Ginseng, but are not an herb or herbal ingredient derived from a plant classified within the genus Panax.

24612×

UNSFDIETUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a dietary supplement or contain a dietary ingredient that renders it adulterated under section 402(a)(1) under the conditions of use recommended or suggested in the labeling of such dietary supplement.

3202×

LACKS FIRM

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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

31201×

EPHEDALK

The product is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a dietary supplement or a dietary ingredient that appears to contain ephedrine alkaloids, which presents an unreasonable risk of illness or injury under the conditions of use recommended or suggested in the labeling, or if no conditions of use are suggested in the labeling, under ordinary conditions of use.

751×

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).

Refusal History

DateProductViolationsDivision
9/29/2016
42OBT01TEAS
482NUTRIT LBL
San Francisco District Office (SAN-DO)
9/29/2016
42OHT01TEAS
482NUTRIT LBL
San Francisco District Office (SAN-DO)
9/29/2016
42OGT01TEAS
482NUTRIT LBL
San Francisco District Office (SAN-DO)
3/4/2016
54FBT44ELEUTHEROCOCCUS (HERBAL & BOTANICALS, NOT TEAS)
3140SBGINSENG
320LACKS FIRM
San Francisco District Office (SAN-DO)
3/4/2016
54FBT44ELEUTHEROCOCCUS (HERBAL & BOTANICALS, NOT TEAS)
3140SBGINSENG
320LACKS FIRM
San Francisco District Office (SAN-DO)
12/3/2015
54FCT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
251POISONOUS
San Francisco District Office (SAN-DO)
12/3/2015
54FCT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
251POISONOUS
San Francisco District Office (SAN-DO)
12/3/2015
54FCT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
251POISONOUS
San Francisco District Office (SAN-DO)
6/29/2015
54FCT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2460UNSFDIETLB
San Francisco District Office (SAN-DO)
6/3/2015
54FCT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2460UNSFDIETLB
San Francisco District Office (SAN-DO)
2/2/2015
54FCT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2460UNSFDIETLB
San Francisco District Office (SAN-DO)
2/2/2015
54FCT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2460UNSFDIETLB
San Francisco District Office (SAN-DO)
11/15/2012
54ECT99HERBALS & BOTANICAL TEAS, N.E.C.
251POISONOUS
San Francisco District Office (SAN-DO)
8/6/2012
54ECT99HERBALS & BOTANICAL TEAS, N.E.C.
251POISONOUS
San Francisco District Office (SAN-DO)
8/6/2012
54ECT99HERBALS & BOTANICAL TEAS, N.E.C.
251POISONOUS
San Francisco District Office (SAN-DO)
8/6/2012
54ECT99HERBALS & BOTANICAL TEAS, N.E.C.
251POISONOUS
San Francisco District Office (SAN-DO)
7/25/2012
54EYT99HERBALS & BOTANICAL TEAS, N.E.C.
2460UNSFDIETLB
2461UNSFDIETUS
251POISONOUS
San Francisco District Office (SAN-DO)
7/25/2012
54EYT99HERBALS & BOTANICAL TEAS, N.E.C.
2460UNSFDIETLB
2461UNSFDIETUS
251POISONOUS
San Francisco District Office (SAN-DO)
7/15/2012
54ECT99HERBALS & BOTANICAL TEAS, N.E.C.
3120EPHEDALK
San Francisco District Office (SAN-DO)
2/28/2002
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Min Tong Pharmaceutical Company's FDA import refusal history?

Min Tong Pharmaceutical Company (FEI: 3003572561) has 20 FDA import refusal record(s) in our database, spanning from 2/28/2002 to 9/29/2016.

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. Min Tong Pharmaceutical Company's FEI number is 3003572561.

What types of violations has Min Tong Pharmaceutical Company received?

Min Tong Pharmaceutical Company 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 Min Tong Pharmaceutical Company come from?

All FDA import refusal data for Min Tong Pharmaceutical Company 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.