The Kilroy Company

Form 483

Mentor, Ohio, United StatesFEI 1527214Issued September 11, 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 1527214.

Observations17

Issue DateSeptember 11, 2009

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: The Kilroy Company
Location: Mentor, Ohio, United States
FEI Number: 1527214
Product Type: Devices
Issue Date: September 11, 2009
Country: United States

Inspection History, 2009 to 2011

NAI1

VAI2

NAI means No Action Indicated. VAI means Voluntary 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.

The Kilroy Company FDA Form 483, Mentor, Ohio, September 11, 2009