FDA Inspection 773213 — Kinamed Inc

Kinamed Inc — FEI 2027148

The FDA completed an inspection of Kinamed Inc on March 15, 2012 in Camarillo, 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
March 15, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Camarillo, CA (United States)