Labverity
Facility profile

STERIS Corporation

FDA-registered facility · St. Louis, MO

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed2 registered company locations
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

Label
Due diligence

Regulatory record at a glance

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Nov 6, 2023 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

Understand this record

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Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

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Ask what was corrected and review any later inspection or follow-up record.

Method and source details
View full inspection and compliance history9 inspection records

FDA inspection history

9 records, Jul 2009 – Nov 2023 · 5 NAI · 4 VAI · 0 OAI

DateClassProject areaCitationsFY
Nov 6, 2023VAIDrug Quality Assurance2024
Jun 8, 2016NAICompliance: Devices2016
Feb 27, 2015VAIDrug Quality AssuranceYes2015
Feb 27, 2015NAIPostmarket Assurance: DevicesYes2015
Feb 27, 2015NAICompliance: DevicesYes2015
May 17, 2011NAICompliance: Devices2011
May 17, 2011NAIDrug Quality Assurance2011
Jul 16, 2009VAICompliance: Devices2009
Jul 16, 2009VAIDrug Quality Assurance2009

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

No warning letter, injunction, or seizure is matched in the current data set.

Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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