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 1000116180.
Observations3
Issue DateDecember 13, 2023
StatusNo Warning Letter
Related Inspections2
Establishment Details
Firm
Midwest Eye Laboratories Inc
Location
Rochester, Minnesota, United States
FEI Number
1000116180
Product Type
Devices
Issue Date
December 13, 2023
Country
United States
Inspection History, 2009 to 2023
NAI1
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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