Cleveland Medical Devices Inc

Form 483

Cleveland, Ohio, United StatesFEI 3000206198Issued July 07, 2017

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 3000206198.

Observations7

Issue DateJuly 07, 2017

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Cleveland Medical Devices Inc
Location: Cleveland, Ohio, United States
FEI Number: 3000206198
Product Type: Devices
Issue Date: July 07, 2017
Country: United States

Inspection History, 2011 to 2026

NAI1

VAI3

OAI1

NAI means No Action Indicated. 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.

Cleveland Medical Devices Inc FDA Form 483, Cleveland, Ohio, July 7, 2017