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 3005651716.
Observations4
Issue DateJuly 26, 2019
StatusNo Warning Letter
Related Inspections7
Establishment Details
Firm
Eurofins Viracor, LLC.
Location
Lenexa, Kansas, United States
FEI Number
3005651716
Product Type
Devices
Issue Date
July 26, 2019
Country
United States
Inspection History, 2010 to 2025
NAI5
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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