M.E.E.I. Boston Keratoprosthesis

Form 483

Boston, Massachusetts, United StatesFEI 1000120597Issued November 20, 2012

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 1000120597.

Observations1

Issue DateNovember 20, 2012

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: M.E.E.I. Boston Keratoprosthesis
Location: Boston, Massachusetts, United States
FEI Number: 1000120597
Product Type: Devices
Issue Date: November 20, 2012
Country: United States

Inspection History, 2009 to 2017

NAI2

VAI1

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.

M.E.E.I. Boston Keratoprosthesis FDA Form 483, Boston, Massachusetts, November 20, 2012