FDA Inspection 685793 — Richmond Diagnostics, Inc.

Richmond Diagnostics, Inc. — FEI 3000206772

The FDA completed an inspection of Richmond Diagnostics, Inc. on October 18, 2010 in North Brunswick, NJ. 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
October 18, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
North Brunswick, NJ (United States)