EPA v. Aeris Air Lite Air Purifiers (COVID-19)
Final Order No Penalty
Case summary
The U.S. Environmental Protection Agency, Region 9 (EPA) is informing the Bureau of Customs and Border Protection of the U.S. Department of Homeland Security (CBP) that the following pesticide device import product in the shipment should be Denied Entry Refused Delivery into the United States pursuant to the authority of Section 17(c) of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), 7 U.S.C. Section 136o(c), and the implementing regulations at 19 C.F.R. Section 12.114.
Defendants (1)
- Aeris Health, IncNamed in complaintNamed in settlement
Facilities (1)
AERIS HEALTH INC
6780 KATELLA AVE., CYPRESS, CA, 90630
Registry ID: 110071091118
Statutes cited
- FIFRA 12A2N — Failure to File Reports
- FIFRA 12A1F — Device Misbranded
Enforcement conclusions (1)
Aeris Air Lite Air Purifiers (COVID-19)entered 2021-09-29
Primary law: FIFRA
Timeline (3 milestones)
- 2021-09-29Enforcement Action Closed
- 2021-09-29Final Order Issued
- 2021-10-05Enforcement Action Data Entered
Case metadata
- EPA activity ID
- 3602845054
- Case number
- 09-2021-4481
- Lead agency
- EPA
- EPA region
- 09
- Voluntary self-disclosure
- No
- Primary statute
- Failure to File Reports
Sourced verbatim from EPA ECHO Enforcement Case Report for case 09-2021-4481 . Bulk data: ICIS-FEC download summary.
This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.