FDA Inspection 652022 — Aim Medical Technologies

Aim Medical Technologies — FEI 3005254477

The FDA completed an inspection of Aim Medical Technologies on March 3, 2010 in Phoenix, AZ. 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 3, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Phoenix, AZ (United States)