CareFusion 303, Inc.

Form 483

San Diego, California, United StatesFEI 2016493Issued October 08, 2010

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 2016493.

Observations3

Issue DateOctober 08, 2010

StatusNo Warning Letter

Related Inspections8

Establishment Details

Firm: CareFusion 303, Inc.
Location: San Diego, California, United States
FEI Number: 2016493
Product Type: Devices
Issue Date: October 08, 2010
Country: United States

Inspection History, 2010 to 2024

NAI1

VAI1

OAI6

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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CareFusion 303, Inc. FDA Form 483, San Diego, California, October 8, 2010