FDA Inspection 1211481 — Midwest Eye Laboratories Sioux Falls, LLC

Midwest Eye Laboratories Sioux Falls, LLC — FEI 1000116181

The FDA completed an inspection of Midwest Eye Laboratories Sioux Falls, LLC on July 27, 2023 in Sioux Falls, SD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 27, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Sioux Falls, SD (United States)