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Evoqua Water Technologies, LLC

FDA Regulatory Profile

Evoqua Water Technologies, LLC has 0 FDA recalls, 19 inspections, 2 510(k) clearances and 1 compliance action on record.

Latest inspection
Feb 4, 2025 · VAI
Latest 510(k)
Jul 19, 2023

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances2Nov 8, 2026File dated Nov 2, 2026Current
Inspections19Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 4, 2025South Windsor, CTDevicesVoluntary Action Indicated (VAI)3006029151
May 14, 2024Buena Park, CADevicesNo Action Indicated (NAI)3009553888
Feb 24, 2022Lowell, MADevicesVoluntary Action Indicated (VAI)3005976438
Dec 13, 2018Dallas, TXDevicesVoluntary Action Indicated (VAI)3007242843
Jun 25, 2018Dallas, TXDevicesOfficial Action Indicated (OAI)3007242843
Jul 13, 2017Minneapolis, MNDevicesNo Action Indicated (NAI)3006475063
Jun 27, 2017Indianapolis, INDevicesNo Action Indicated (NAI)3004057358
Jun 13, 2017Lowell, MADevicesNo Action Indicated (NAI)3005976438
Mar 2, 2016San Antonio, TXDevicesNo Action Indicated (NAI)3001481133
Jul 21, 2015Buena Park, CADevicesNo Action Indicated (NAI)3009553888
Dec 4, 2014Minneapolis, MNDevicesNo Action Indicated (NAI)3006475063
Feb 18, 2014Minneapolis, MNDevicesVoluntary Action Indicated (VAI)3006475063
Jun 24, 2013Buena Park, CADevicesNo Action Indicated (NAI)3009553888
Feb 20, 2013Indianapolis, INDevicesNo Action Indicated (NAI)3004057358
Nov 28, 2012Lowell, MADevicesVoluntary Action Indicated (VAI)3005976438
Apr 9, 2012Indianapolis, INDevicesOfficial Action Indicated (OAI)3004057358
Mar 15, 2012San Antonio, TXDevicesVoluntary Action Indicated (VAI)3001481133
May 25, 2011South Windsor, CTDevicesNo Action Indicated (NAI)3006029151
Mar 2, 2011North Chesterfield, VADevicesNo Action Indicated (NAI)3008155529

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3006029151South Windsor, CT2Feb 4, 2025
FEI 3009553888Buena Park, CA3May 14, 2024
FEI 3005976438Lowell, MA3Feb 24, 2022
FEI 3007242843Dallas, TX2Dec 13, 2018
FEI 3006475063Minneapolis, MN3Jul 13, 2017
FEI 3004057358Indianapolis, IN3Jun 27, 2017
FEI 3001481133San Antonio, TX2Mar 2, 2016
FEI 3008155529North Chesterfield, VA1Mar 2, 2011

Recent 510(k) Clearances

K-NumberDeviceDate
K231410RenaPure Endotoxin Retentive FilterJul 19, 2023
K153784NOSOGARD FILTERSOct 21, 2016

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.