FDA Inspection 1274217 — Tissue Regenix, Inc.

Tissue Regenix, Inc. — FEI 3026672062

The FDA completed an inspection of Tissue Regenix, Inc. on June 24, 2025 in Buford, GA. 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
June 24, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Buford, GA (United States)