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 3009498109.
Observations3
Issue DateJune 26, 2017
StatusNo Warning Letter
Related Inspections2
Establishment Details
Firm
MyCardio
Location
Denver, Colorado, United States
FEI Number
3009498109
Product Type
Devices
Issue Date
June 26, 2017
Country
United States
Inspection History, 2012 to 2017
NAI1
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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