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 3013957857.
Observations1
Issue DateMay 23, 2019
StatusNo Warning Letter
Establishment TypeManufacturer
Related Inspections2
Establishment Details
Firm
Liveyon
Location
Yorba Linda, California, United States
FEI Number
3013957857
Establishment Type
Manufacturer
Product Type
Drugs
Issue Date
May 23, 2019
Country
United States
Inspection History, 2018 to 2019
VAI1
OAI1
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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