Kimberly-Clark Corporation
⚠️ Moderate Risk
FEI: 1000015879 • Roswell, GA • UNITED STATES
FEI Number
1000015879
Location
Roswell, GA
Country
UNITED STATESAddress
1400 Holcomb Bridge Rd, , Roswell, GA, United States
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).
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/17/2018 | 80FMCGLOVE, PATIENT EXAMINATION | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 12/17/2018 | 80FMCGLOVE, PATIENT EXAMINATION | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 12/17/2018 | 80FMCGLOVE, PATIENT EXAMINATION | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 7/2/2008 | 80NZJRESPIRATOR, N95, HOME USE | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Kimberly-Clark Corporation's FDA import refusal history?
Kimberly-Clark Corporation (FEI: 1000015879) has 4 FDA import refusal record(s) in our database, spanning from 7/2/2008 to 12/17/2018.
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. Kimberly-Clark Corporation's FEI number is 1000015879.
What types of violations has Kimberly-Clark Corporation received?
Kimberly-Clark Corporation has been cited for 2 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 Kimberly-Clark Corporation come from?
All FDA import refusal data for Kimberly-Clark Corporation 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.