FDA Inspection 1112312 — Scendia Biologics, LLC

Scendia Biologics, LLC — FEI 3012807083

The FDA completed an inspection of Scendia Biologics, LLC on Nov 13, 2019 in Orlando, 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
Nov 13, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Orlando, FL (United States)

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