FDA Inspection 629447 — Aktina Medical Corp

Aktina Medical Corp — FEI 1000521490

The FDA completed an inspection of Aktina Medical Corp on November 6, 2009 in Congers, NY. 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
November 6, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Congers, NY (United States)