FDA Inspection 1265138 — Ataia, Inc

Ataia, Inc — FEI 3016096197

The FDA completed an inspection of Ataia, Inc on March 24, 2025 in Columbia, MD. 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
March 24, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbia, MD (United States)