FDA Inspection 582250 — Midwest Eye Laboratories Inc
The FDA completed an inspection of Midwest Eye Laboratories Inc on May 11, 2009 in Rochester, 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
- May 11, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Rochester, MN (United States)