FDA Inspection 1116156 — TForce

TForce — FEI 3013678325

The FDA completed an inspection of TForce on January 23, 2020 in Saint Louis, MO. 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, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Saint Louis, MO (United States)