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Lanzhou Taibao Pharmaceutical Company, LLC

⚠️ Moderate Risk

FEI: 1000577653 • Lanzhou, Gansu • CHINA

FEI

FEI Number

1000577653

📍

Location

Lanzhou, Gansu

🇨🇳

Country

CHINA
🏢

Address

No. 85 Jian West West Rd, , Lanzhou, Gansu, China

Moderate Risk

FDA Import Risk Assessment

41.0
LowModerateHighCritical

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

Statistics

18
Total Refusals
6
Unique Violations
12/7/2018
Latest Refusal
8/12/2005
Earliest Refusal

Score Breakdown

Violation Severity
63.7×40%
Refusal Volume
47.4×30%
Recency
0.0×20%
Frequency
13.5×10%
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

7511×

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).

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).

4826×

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.

4833×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

2561×

INCONSPICU

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)).

Refusal History

DateProductViolationsDivision
12/7/2018
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of West Coast Imports (DWCI)
9/13/2016
54FCT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
256INCONSPICU
482NUTRIT LBL
San Francisco District Office (SAN-DO)
1/22/2013
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
1/22/2013
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
1/22/2013
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
1/22/2013
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
1/22/2013
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
5/25/2012
54ECR99HERBALS & BOTANICAL TEAS, N.E.C.
482NUTRIT LBL
New York District Office (NYK-DO)
4/6/2011
54FAR99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
New York District Office (NYK-DO)
1/20/2011
54FAR99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
482NUTRIT LBL
New York District Office (NYK-DO)
1/20/2011
54FAR99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
482NUTRIT LBL
New York District Office (NYK-DO)
1/20/2011
54FAR99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
482NUTRIT LBL
New York District Office (NYK-DO)
1/20/2011
54FAR99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
482NUTRIT LBL
New York District Office (NYK-DO)
12/10/2008
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/16/2008
54YCT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
249FILTHY
San Francisco District Office (SAN-DO)
8/12/2005
60LAB99ANALGESIC, N.E.C.
118NOT LISTED
483DRUG NAME
75UNAPPROVED
San Francisco District Office (SAN-DO)
8/12/2005
60LAB99ANALGESIC, N.E.C.
118NOT LISTED
483DRUG NAME
75UNAPPROVED
San Francisco District Office (SAN-DO)
8/12/2005
65VAB99SEDATIVE N.E.C.
118NOT LISTED
483DRUG NAME
75UNAPPROVED
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Lanzhou Taibao Pharmaceutical Company, LLC's FDA import refusal history?

Lanzhou Taibao Pharmaceutical Company, LLC (FEI: 1000577653) has 18 FDA import refusal record(s) in our database, spanning from 8/12/2005 to 12/7/2018.

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. Lanzhou Taibao Pharmaceutical Company, LLC's FEI number is 1000577653.

What types of violations has Lanzhou Taibao Pharmaceutical Company, LLC received?

Lanzhou Taibao Pharmaceutical Company, LLC has been cited for 6 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 Lanzhou Taibao Pharmaceutical Company, LLC come from?

All FDA import refusal data for Lanzhou Taibao Pharmaceutical Company, LLC 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.