FDA Inspection 874159 — Sonablate Corp.

Sonablate Corp. — FEI 3007126306

The FDA completed an inspection of Sonablate Corp. on Mar 26, 2014 in Charlotte, NC. 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
Mar 26, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Charlotte, NC (United States)

Additional Details

Sponsor, Contract Research Organization