FDA Inspection 774767 — Midwest Eye Laboratories Woodbury, LLC

Midwest Eye Laboratories Woodbury, LLC — FEI 2183831

The FDA completed an inspection of Midwest Eye Laboratories Woodbury, LLC on Mar 27, 2012 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 27, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)