FDA Inspection 764115 — Visicu, Inc.

Visicu, Inc. — FEI 3003063823

The FDA completed an inspection of Visicu, Inc. on Jan 11, 2012 in Baltimore, 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
Jan 11, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Baltimore, MD (United States)