FDA Inspection 1276689 — Richmond Diagnostics, Inc.

Richmond Diagnostics, Inc. — FEI 3000206772

The FDA completed an inspection of Richmond Diagnostics, Inc. on July 25, 2025 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). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 25, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
North Brunswick, NJ (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
315921 CFR 820.184DHR content
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures