FDA Inspection 561508 — LISI MEDICAL Remmele, Inc.
The FDA completed an inspection of LISI MEDICAL Remmele, Inc. on Feb 4, 2009 in Coon Rapids, 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
- Feb 4, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Coon Rapids, MN (United States)