FDA Inspection 1236951 — Ameditech Inc

Ameditech Inc — FEI 3003789989

The FDA completed an inspection of Ameditech Inc on August 16, 2024 in San Diego, CA. 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
August 16, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)