Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3000206772.
Observations1
Issue DateAugust 21, 2017
StatusNo Warning Letter
Related Inspections4
Establishment Details
Firm
Richmond Diagnostics, Inc.
Location
North Brunswick, New Jersey, United States
FEI Number
3000206772
Product Type
Devices
Issue Date
August 21, 2017
Country
United States
Inspection History, 2010 to 2025
NAI2
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
Talk to a Specialist