FDA Inspection 681628 — Ameditech Inc

Ameditech Inc — FEI 3003789989

The FDA completed an inspection of Ameditech Inc on September 23, 2010 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
September 23, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)