Home / Inspections / 1042349

FDA Inspection 1042349 — 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 February 15, 2018 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
February 15, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Sioux Falls, SD (United States)

Facility

Other inspections at this facility

  • 1211481 (NAI Thu Jul 27 2023 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources