FDA Inspection 1084184 — LifeBridge Health, Inc. IRB

LifeBridge Health, Inc. IRB — FEI 3004059642

The FDA completed an inspection of LifeBridge Health, Inc. IRB on March 13, 2019 in Baltimore, MD. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 13, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Baltimore, MD (United States)

Additional Details

IRB