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 3013341563.
Observations8
Issue DateMay 24, 2017
Status1 Related Warning Letter
Establishment TypeProducer of Sterile Drug Products
Related Inspections0
Establishment Details
Firm
Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical
Location
California, United States
FEI Number
3013341563
Establishment Type
Producer of Sterile Drug Products
Product Type
Drugs
Issue Date
May 24, 2017
Country
United States
Inspection History
We hold no FDA inspection matched to this establishment.
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