FDA Inspection 1271183 — Tendonova Corporation

Tendonova Corporation — FEI 3025663926

The FDA completed an inspection of Tendonova Corporation on May 16, 2025 in Atlanta, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 16, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Atlanta, GA (United States)