Ziehm Imaging Gmbh

Form 483

Nuremberg, -, GermanyFEI 3005430103Issued February 17, 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 3005430103.

Observations2

Issue DateFebruary 17, 2017

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Ziehm Imaging Gmbh
Location: Nuremberg, -, Germany
FEI Number: 3005430103
Product Type: Devices
Issue Date: February 17, 2017
Country: Germany

Inspection History, 2012 to 2017

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.

Ziehm Imaging Gmbh FDA Form 483, Nuremberg, February 17, 2017