Dornier Medtech Laser GmbH

Form 483

Wesling, -, GermanyFEI 3002807538Issued July 31, 2014

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 3002807538.

Observations1

Issue DateJuly 31, 2014

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Dornier Medtech Laser GmbH
Location: Wesling, -, Germany
FEI Number: 3002807538
Product Type: Devices
Issue Date: July 31, 2014
Country: Germany

Inspection History, 2014 to 2017

NAI1

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.

Dornier Medtech Laser GmbH FDA Form 483, Wesling, July 31, 2014