Min Tong Pharmaceutical Company
⚠️ Moderate Risk
FEI: 3003572561 • Taichung • TAIWAN
FEI Number
3003572561
Location
Taichung
Country
TAIWANAddress
Factory 15, 21 St Road, Industrial Zone, , Taichung, , Taiwan
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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:
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.
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.
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.
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.
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.
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 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) | San Francisco District Office (SAN-DO) | |
| 3/4/2016 | 54FBT44ELEUTHEROCOCCUS (HERBAL & BOTANICALS, NOT TEAS) | 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. | San Francisco District Office (SAN-DO) | |
| 7/25/2012 | 54EYT99HERBALS & BOTANICAL TEAS, N.E.C. | 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.