FDA Inspection 1178135 — TeVido BioDevices Inc

TeVido BioDevices Inc — FEI 3013075151

The FDA completed an inspection of TeVido BioDevices Inc on Aug 8, 2022 in Austin, TX. 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
Aug 8, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Austin, TX (United States)