FDA Inspection 831718 — IntegReview, Inc. IRB

IntegReview, Inc. IRB — FEI 3003943497

The FDA completed an inspection of IntegReview, Inc. IRB on May 15, 2013 in Austin, TX. 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
May 15, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Austin, TX (United States)

Additional Details

IRB