Ahlstrom Nonwovens, LLC

FDA Regulatory Profile

Ahlstrom Nonwovens, LLC has 0 FDA recalls, 6 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Feb 21, 2025 · NAI
Latest 510(k)
Jun 29, 2017

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances2Oct 4, 2026Not statedCurrent
Inspections6Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 21, 2025Windsor Locks, CTDevicesNo Action Indicated (NAI)1217231
Mar 21, 2018Windsor Locks, CTDevicesVoluntary Action Indicated (VAI)1217231
May 13, 2014Windsor Locks, CTDevicesVoluntary Action Indicated (VAI)1217231
May 13, 2014Windsor Locks, CTDevicesVoluntary Action Indicated (VAI)1217231
Aug 1, 2011Windsor Locks, CTDevicesNo Action Indicated (NAI)1217231
Jul 29, 2011Windsor Locks, CTDevicesNo Action Indicated (NAI)1217231

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.

Recent 510(k) Clearances

K-NumberDeviceDate
K171533Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization WrapJun 29, 2017
K160755Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization WrapJul 27, 2016