FDA Inspection 685793 — Richmond Diagnostics, Inc.

Richmond Diagnostics, Inc. — FEI 3000206772

The FDA completed an inspection of Richmond Diagnostics, Inc. on Oct 18, 2010 in North Brunswick, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 18, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
North Brunswick, NJ (United States)

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