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 3017600845.
Observations6
Issue DateMarch 18, 2022
StatusNo Warning Letter
Establishment TypeProducer of Sterile Drug Products
Related Inspections0
Establishment Details
Firm
Optum Infusion 483 Issued 03/18/2022
Location
Arizona, United States
FEI Number
3017600845
Establishment Type
Producer of Sterile Drug Products
Issue Date
March 18, 2022
Country
United States
Inspection History
We hold no FDA inspection matched to this establishment.
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