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 3002757762.
Observations3
Issue DateSeptember 21, 2018
StatusNo Warning Letter
Related Inspections4
Establishment Details
Firm
Vitrolife Inc.
Location
San Diego, California, United States
FEI Number
3002757762
Product Type
Devices
Issue Date
September 21, 2018
Country
United States
Inspection History, 2014 to 2025
NAI2
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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