FDA Inspection 1001761 — AdventHealth, Daytona Beach

AdventHealth, Daytona Beach — FEI 3008736453

The FDA completed an inspection of AdventHealth, Daytona Beach on Jan 12, 2017 in Daytona Beach, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 12, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Daytona Beach, FL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.