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Avista Pharma Solutions, Inc.

FDA Regulatory Profile

Avista Pharma Solutions, Inc. has 0 FDA recalls, 11 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jul 25, 2025 · VAI

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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) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections11Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 25, 2025Agawam, MADrugsVoluntary Action Indicated (VAI)1220785
Jul 3, 2025Durham, NCDrugsNo Action Indicated (NAI)3011795391
May 3, 2024Longmont, CODrugsVoluntary Action Indicated (VAI)3012316957
Jul 17, 2020Durham, NCDrugsNo Action Indicated (NAI)3011795391
Dec 18, 2019Agawam, MADrugsVoluntary Action Indicated (VAI)1220785
Sep 5, 2018Agawam, MADrugsNo Action Indicated (NAI)1220785
Jun 15, 2016Agawam, MADrugsVoluntary Action Indicated (VAI)1220785
Sep 27, 2013Agawam, MADrugsVoluntary Action Indicated (VAI)1220785
Oct 30, 2012Durham, NCDrugsNo Action Indicated (NAI)3011795391
Oct 27, 2010Agawam, MADrugsNo Action Indicated (NAI)1220785
Oct 9, 2009Durham, NCDrugsNo Action Indicated (NAI)3011795391

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 1220785Agawam, MA6Jul 25, 2025
FEI 3011795391Durham, NC4Jul 3, 2025
FEI 3012316957Longmont, CO1May 3, 2024

FDA data resources

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