Siemens Healthcare Diagnostics, Inc.

Form 483

Newark, Delaware, United StatesFEI 2517506Issued February 09, 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 2517506.

Observations3

Issue DateFebruary 09, 2012

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Siemens Healthcare Diagnostics, Inc.
Location: Newark, Delaware, United States
FEI Number: 2517506
Product Type: Devices
Issue Date: February 09, 2012
Country: United States

Inspection History, 2009 to 2014

NAI1

VAI2

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.

Siemens Healthcare Diagnostics, Inc. FDA Form 483, Newark, Delaware, February 9, 2012