FDA Inspection 708949 — Alara Incorporated

Alara Incorporated — FEI 3001253987

The FDA completed an inspection of Alara Incorporated on February 9, 2011 in Fremont, 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
February 9, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Fremont, CA (United States)