FDA Inspection 910759 — LISI MEDICAL Remmele, Inc
The FDA completed an inspection of LISI MEDICAL Remmele, Inc on Jan 14, 2015 in Big Lake, 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
- Jan 14, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Big Lake, MN (United States)