FDA Inspection 648551 — Westat Inc

Westat Inc — FEI 3010224798

The FDA completed an inspection of Westat Inc on Feb 16, 2010 in Rockville, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 16, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Rockville, MD (United States)

Additional Details

Sponsor, Contract Research Organization