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 3009161688.
Observations1
Issue DateOctober 10, 2024
StatusNo Warning Letter
Related Inspections2
Establishment Details
Firm
Veridiam, Inc.
Location
El Cajon, California, United States
FEI Number
3009161688
Product Type
Devices
Issue Date
October 10, 2024
Country
United States
Inspection History, 2014 to 2024
NAI1
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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