FDA Inspection 1078122 — AdventHealth, Daytona Beach

AdventHealth, Daytona Beach — FEI 3008736453

The FDA completed an inspection of AdventHealth, Daytona Beach on January 23, 2019 in Daytona Beach, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 23, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Daytona Beach, FL (United States)