FDA Inspection 612689 — AKSM/GOULD INC

AKSM/GOULD INC — FEI 3005893994

The FDA completed an inspection of AKSM/GOULD INC on July 27, 2009 in Columbus, OH. 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
July 27, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbus, OH (United States)