Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 2016493.
Observations8
Issue DateApril 06, 2020
StatusNo Warning Letter
Establishment TypeMedical Device Manufacturer
Related Inspections8
Establishment Details
Firm
CareFusion 303, Inc.
Location
San Diego, California, United States
FEI Number
2016493
Establishment Type
Medical Device Manufacturer
Product Type
Devices
Issue Date
April 06, 2020
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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