Steris Corporation

Form 483

Mentor, Ohio, United StatesFEI 1527821Issued November 06, 2009

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1527821.

Observations3

Issue DateNovember 06, 2009

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Steris Corporation
Location: Mentor, Ohio, United States
FEI Number: 1527821
Product Type: Devices
Issue Date: November 06, 2009
Country: United States

Inspection History, 2009 to 2020

VAI4

OAI1

VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Steris Corporation FDA Form 483, Mentor, Ohio, November 6, 2009