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 3013942511.
Observations2
Issue DateSeptember 23, 2019
StatusNo Warning Letter
Related Inspections5
Establishment Details
Firm
Isopure Corp.
Location
Louisville, Kentucky, United States
FEI Number
3013942511
Product Type
Devices
Issue Date
September 23, 2019
Country
United States
Inspection History, 2011 to 2024
NAI1
VAI4
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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