Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1718873.
Observations7
Issue DateJuly 23, 2015
StatusNo Warning Letter
Establishment TypeMedical Device Manufacturer
Related Inspections2
Establishment Details
Firm
Utah Medical Products, Inc
Location
Midvale, Utah, United States
FEI Number
1718873
Establishment Type
Medical Device Manufacturer
Product Type
Devices
Issue Date
July 23, 2015
Country
United States
Inspection History, 2010 to 2014
NAI1
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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