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 3003274090.
Observations2
Issue DateFebruary 13, 2019
StatusNo Warning Letter
Related Inspections4
Establishment Details
Firm
Vitrolife, Inc.
Location
Englewood, Colorado, United States
FEI Number
3003274090
Product Type
Devices
Issue Date
February 13, 2019
Country
United States
Inspection History, 2010 to 2019
NAI2
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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