Qingdao Qingmei Biotech Co., Ltd.
⚠️ Moderate Risk
FEI: 3011562813 • Qingdao, Shandong • CHINA
FEI Number
3011562813
Location
Qingdao, Shandong
Country
CHINAAddress
6 Hongkong Middle Rd, B203a, Shinan District, Qingdao, Shandong, China
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
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).
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
Frequently Asked Questions
What is Qingdao Qingmei Biotech Co., Ltd.'s FDA import refusal history?
Qingdao Qingmei Biotech Co., Ltd. (FEI: 3011562813) has 1 FDA import refusal record(s) in our database, spanning from 7/26/2017 to 7/26/2017.
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. Qingdao Qingmei Biotech Co., Ltd.'s FEI number is 3011562813.
What types of violations has Qingdao Qingmei Biotech Co., Ltd. received?
Qingdao Qingmei Biotech Co., Ltd. has been cited for 3 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 Qingdao Qingmei Biotech Co., Ltd. come from?
All FDA import refusal data for Qingdao Qingmei Biotech 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.